Fusion proteins and methods thereof

ABSTRACT

The invention discloses oncogenic fusion proteins. The invention provides methods for treating gene-fusion based cancers.

The application is a continuation of PCT International Application No. PCT/US2014/026351 filed on Mar. 13, 2014, which claims the benefit of and priority to U.S. Provisional Patent Application No. 61/793,086, filed on Mar. 15, 2013, the content of which are hereby incorporated by reference in their entireties.

All patents, patent applications and publications cited herein are hereby incorporated by reference in their entirety. The disclosures of these publications in their entireties are hereby incorporated by reference into this application.

This patent disclosure contains material that is subject to copyright protection. The copyright owner has no objection to the facsimile reproduction by anyone of the patent document or the patent disclosure as it appears in the U.S. Patent and Trademark Office patent file or records, but otherwise reserves any and all copyright rights.

GOVERNMENT SUPPORT

This invention was made with government support under Grant No. R01CA101644 awarded by the National Cancer Institute. The Government has certain rights in the invention.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Nov. 23, 2015, is named 19240.1034US2_SL.txt and is 2,208,530 bytes in size.

BACKGROUND OF THE INVENTION

Glioblastoma multiforme (GBM) is the most common form of brain cancer and among the most incurable and lethal of all human cancers. The current standard of care includes surgery, chemotherapy, and radiation therapy. However, the prognosis of GBM remains uniformly poor. There are few available targeted therapies and none that specifically target GBM.

The target population of GBM patients who may carry EGFR gene fusions and would benefit from targeted inhibition of EGFR kinase activity is estimated to correspond to 6,000 patients per year world-wide.

SUMMARY OF THE INVENTION

The invention is based, at least in part, on the discovery of a highly expressed class of gene fusions in GBM, which join the receptor tyrosine kinase (RTK) domain of EGFR genes to the coiled-coil domain of septin proteins, such as Septin-14, or fused to a polypeptide comprising a phosphoserine phosphatase (PSPH) protein or a polypeptide comprising a Cullin-associated and neddylation-dissociated (CAND) protein. The invention is based, at least in part, on the finding that EGFR-SEPT fusions, EGFR-PSPH fusions, and EGFR-CAND fusions identify a subset of GBM patients who will benefit from targeted inhibition of the tyrosine kinase activity of EGFR. Identification of fusions of EGFR genes in glioblastoma patients are useful therapeutic targets.

An aspect of the invention is directed to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified fusion protein comprising the tyrosine kinase domain of an EGFR protein fused 5′ to a polypeptide comprising the coiled-coil domain of a Septin protein. In one embodiment, the Septin protein is Septin-1, Septin-2, Septin-3, Septin-4, Septin-5, Septin-6, Septin-7, Septin-8, Septin-9, Septin-10, Septin-11, Septin-12, Septin-13, or Septin-14. In another embodiment, the Septin protein is Septin-14 (SEPT14). In another embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified fusion protein comprising the tyrosine kinase domain of an EGFR protein fused 5′ to a polypeptide comprising a phosphoserine phosphatase (PSPH) protein. In another embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified fusion protein comprising the tyrosine kinase domain of an EGFR protein fused 3′ to a polypeptide comprising a Cullin-associated and neddylation-dissociated (CAND) protein. In one embodiment, the CAND protein is CAND1, CAND2, or CAND3. In another embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified fusion protein encoded by an EGFR-SEPT14 nucleic acid, wherein EGFR-SEPT14 comprises a combination of exons 1-25 of EGFR located on human chromosome 7p11.2 spliced 5′ to a combination of exons 7-10 of SEPT14 located on human chromosome 7, wherein a genomic breakpoint occurs in any one of exons 1-25 of EGFR and any one of exons 7-10 of SEPT14. In another embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified fusion protein encoded by an EGFR-PSPH nucleic acid, wherein EGFR-PSPH comprises a combination of exons 1-25 of EGFR located on human chromosome 7p12 spliced 5′ to a combination of exons 1-10 of PSPH located on human chromosome 7p11.2, wherein a genomic breakpoint occurs in any one of exons 1-25 of EGFR and any one of exons 1-10 of PSPH. In another embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified fusion protein encoded by an EGFR-CAND1 nucleic acid, wherein EGFR-CAND1 comprises a combination of exons 1-25 of EGFR located on human chromosome 7p12 spliced 3′ to a combination of exons 1-16 of CAND1 located on human chromosome 12q14, wherein a genomic breakpoint occurs in any one of exons 1-25 of EGFR and any one of exons 1-16 of CAND1. In another embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a synthetic nucleic acid encoding the EGFR fusion proteins described above.

An aspect of the invention is directed to a purified EGFR-SEPT14 fusion protein comprising SEQ ID NO: 1 or 5. In one embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified EGFR-SEPT14 fusion protein having a genomic breakpoint comprising SEQ ID NO: 4. In another embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified EGFR-PSPH fusion protein comprising SEQ ID NO: 7 or 11. In another embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified EGFR-PSPH fusion protein having a genomic breakpoint comprising SEQ ID NO: 10. In one embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified EGFR-CAND1 fusion protein comprising SEQ ID NO: 13 or 8495. In one embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a purified EGFR-CAND1 fusion protein having a genomic breakpoint comprising SEQ ID NO: 15. In one embodiment, the purified fusion protein is essentially free of other human proteins.

An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-SEPT14 fusion protein comprising SEQ ID NO: 2.

An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-SEPT14 fusion protein having a genomic breakpoint comprising SEQ ID NO: 4.

An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-PSPH fusion protein comprising SEQ ID NO: 8.

An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-PSPH fusion protein having a genomic breakpoint comprising SEQ ID NO: 10.

An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-CAND1 fusion protein comprising SEQ ID NO: 14.

An aspect of the invention is directed to a synthetic nucleic acid encoding an EGFR-CAND1 fusion protein having a genomic breakpoint comprising SEQ ID NO: 15.

An aspect of the invention is directed to an antibody or antigen-binding fragment thereof that specifically binds to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the fusion protein is an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND fusion protein. In another embodiment, the EGFR-SEPT fusion protein is EGFR-SEPT14. In one embodiment, the EGFR-SEPT fusion protein comprises the amino acid sequence of SEQ ID NO: 1, 3, or 5. In one embodiment, the EGFR-CAND fusion protein is EGFR-CAND1. In one embodiment, the EGFR-CAND fusion protein comprises the amino acid sequence of SEQ ID NO: 13, 16, or 8495.

An aspect of the invention is directed to an antibody or antigen-binding fragment thereof that specifically binds to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide comprising the coiled-coil domain of a Septin protein. In another embodiment, the EGFR-SEPT fusion protein is EGFR-SEPT14. In one embodiment, the EGFR-SEPT fusion protein comprises the amino acid sequence of SEQ ID NO: 1, 3, or 5.

An aspect of the invention is directed to an antibody or antigen-binding fragment thereof that specifically binds to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide comprising a phosphoserine phosphatase (PSPH) protein. In one embodiment, the EGFR-PSPH fusion protein comprises the amino acid sequence of SEQ ID NO: 7, 9, or 11.

An aspect of the invention is directed to an antibody or antigen-binding fragment thereof, that specifically binds to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide comprising a Cullin-associated and neddylation-dissociated (CAND) protein. In one embodiment, the EGFR-CAND fusion protein is EGFR-CAND1. In one embodiment, the EGFR-CAND fusion protein comprises the amino acid sequence of SEQ ID NO: 13, 16, or 8495.

An aspect of the invention is directed to a composition for decreasing the expression level or activity of a fusion protein in a subject comprising the tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein, the composition in an admixture of a pharmaceutically acceptable carrier comprising an inhibitor of the fusion protein. In one embodiment, the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof. In another embodiment, the CAND protein is CAND1. In a further embodiment, the SEPT protein is SEPT14. In some embodiments, the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.

An aspect of the invention is directed to a method for treating a gene-fusion associated cancer in a subject in need thereof, the method comprising administering to the subject an effective amount of an EGFR fusion molecule inhibitor. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the EGFR fusion comprises an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the EGFR fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In one embodiment, the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof. In one embodiment, the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.

An aspect of the invention is directed to a method of decreasing growth of a solid tumor in a subject in need thereof, the method comprising administering to the subject an effective amount of an EGFR fusion molecule inhibitor, wherein the inhibitor decreases the size of the solid tumor. In one embodiment, the subject is afflicted with a gene-fusion associated cancer. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the solid tumor comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the EGFR fusion comprises an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the EGFR fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In one embodiment, the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof. In one embodiment, the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.

An aspect of the invention is directed to a method of reducing cell proliferation in a subject afflicted with a gene-fusion associated cancer, the method comprising administering to the subject an effective amount of an EGFR fusion molecule inhibitor, wherein the inhibitor decreases cell proliferation. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the EGFR fusion comprises an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In one embodiment, the EGFR fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In one embodiment, the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof. In one embodiment, the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.

An aspect of the invention is directed to a diagnostic kit for determining whether a sample from a subject exhibits a presence of an EGFR fusion, the kit comprising at least one oligonucleotide that specifically hybridizes to an EGFR fusion, or a portion thereof. In one embodiment, the oligonucleotides comprise a set of nucleic acid primers or in situ hybridization probes. In another embodiment, the oligonucleotide comprises SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, 89, or a combination thereof. In a further embodiment, the primers prime a polymerase reaction only when an EGFR fusion is present. In some embodiments, the fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In other embodiments, the determining comprises gene sequencing, selective hybridization, selective amplification, gene expression analysis, or a combination thereof.

An aspect of the invention is directed to a diagnostic kit for determining whether a sample from a subject exhibits a presence of an EGFR fusion protein, the kit comprising an antibody that specifically binds to an EGFR fusion protein comprising SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 16, or 8495, wherein the antibody will recognize the protein only when an EGFR fusion protein is present. In one embodiment, the fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. In one embodiment, the subject is afflicted with a gene-fusion associated cancer. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma.

An aspect of the invention is directed to a method for detecting the presence of an EGFR fusion in a human subject. The method comprises obtaining a biological sample from the human subject; and detecting whether or not there is an EGFR fusion present in the subject. In one embodiment, the detecting comprises measuring EGFR fusion protein levels by ELISA using an antibody directed to SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 16, or 8495; western blot using an antibody directed to SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 16, or 8495; mass spectroscopy, isoelectric focusing, or a combination thereof.

An aspect of the invention is directed to a method for detecting the presence of an EGFR fusion in a human subject. The method comprises obtaining a biological sample from a human subject; and detecting whether or not there is a nucleic acid sequence encoding an EGFR fusion protein in the subject. In one embodiment, the nucleic acid sequence comprises any one of SEQ ID NOS: 2, 4, 8, 10, 14, and 15. In another embodiment, the detecting comprises using hybridization, amplification, or sequencing techniques to detect an EGFR fusion. In a further embodiment, the amplification uses primers comprising SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, or 89. In some embodiments, the fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein.

BRIEF DESCRIPTION OF THE FIGURES

To conform to the requirements for PCT patent applications, many of the figures presented herein are black and white representations of images originally created in color. In the below descriptions and the examples, the colored plots and images are described in terms of its appearance in black and white. The original color versions can be viewed in Frattini et al., (2013) Nature Genetics, 45(10):1141-49 (including the accompanying Supplementary Information available in the on-line version of the manuscript available on the Nature Genetics web site). For the purposes of the PCT, the contents of Frattini et al., (2013) Nature Genetics, 45(10):1141-49, including the accompanying “Supplementary Information,” are herein incorporated by reference.

FIG. 1A is a chromosome view of validated GBM genes scoring at the top of each of the three categories by MutComFocal. The plot shows mutated genes without significant copy number alterations (Mut, mutation %, frequency of mutations). Previously known GBM genes are indicated in green (light grey in black and white image), new and independently validated GBM genes are indicated in red (dark grey in black and white image).

FIG. 1B is a chromosome view of validated GBM genes scoring at the top of each of the three categories by MutComFocal. The plot shows mutated genes in regions of focal and recurrent amplifications (Amp-Mut, Amplification/mutation scores). Previously known GBM genes are indicated in green (light grey in black and white image), new and independently validated GBM genes are indicated in red (dark grey in black and white image).

FIG. 1C is a chromosome view of validated GBM genes scoring at the top of each of the three categories by MutComFocal. The plot shows mutated genes in regions of focal and recurrent deletions (Del-Mut, Deletion/mutation scores). Previously known GBM genes are indicated in green (light grey in black and white image), new and independently validated GBM genes are indicated in red (dark grey in black and white image).

FIGS. 2A-B shows Localization of altered residues in LZTR-1. FIG. 2A shows lysates from 293T cells transfected with vectors expressing LZTR-1 and the Flag-Cul3 wild type (WT), Flag-Cul3-dominant negative (DN) or the empty vector were immunoprecipitated with Flag antibody and assayed by western blot with the indicated antibodies. *, non specific band; left bracket indicates Cul3 polypeptides. The molecular weight is indicated on the right. FIG. 2B shows homology model of the Kelch (green; grey in black and white image of left hand side of ribbon diagram), BTB (cyan; (light grey in black and white image of center and right of ribbon diagram) and BACK (purple; dark grey in black and white image of center and right of ribbon diagram) domains of LZTR-1 with the Cul3 N-terminal domain (white) docked onto the putative binding site. GBM mutations are indicated in red (dark grey in black and white image; left hand side of ribbon diagram).

FIG. 2C. Sequence alignment of the six blades from the Kelch β-propeller domain. Each blade contains four core β-strands, labeled a, b, c, d. Conserved residues are highlighted in gray and residues mutated in GBM are shown in red. Insertions at the end of blades 5 and 6 are indicated in brackets. Figure discloses SEQ ID NO: 8478.

FIGS. 3A-B. Loss of CD drives mesenchymal transformation of GBM. 3 a, Immunofluorescence staining of human brain cortex using δ-catenin antibody (red, left panel); Nuclei are counterstained with Dapi (blue, right panel). 3 b, Immunofluorescence staining of human primary GBM included in tissue microarrays (TMA) using δ-catenin antibody (red); Nuclei are counterstained with Dapi (blue). A representative δ-catenin-positive and negative tumor is shown in the left and right panel, respectively.

FIGS. 3C-D. Loss of CD drives mesenchymal transformation of GBM. 3 c, Kaplan-Meier analysis for glioma patients with low CTNND2 mRNA expression 2-fold, red line) compared with the rest of glioma (blue line). 3 d, Kaplan-Meier analysis for glioma patients with low CTNND2 mRNA expression (2-fold) and decreased CTNND2 gene copy number (1) (red line) compared with the rest of glioma (blue line).

FIGS. 3E-F. Loss of CD drives mesenchymal transformation of GBM. 3 e, Growth rate of U87 glioma cells transduced with a lentivirus expressing δ-catenin (squares) or the empty vector (circles, average of triplicate cultures). 3 f, Expression of mesenchymal genes in glioma cells expressing δ-catenin or the empty vector (averages of triplicate quantitative RT-PCR). All error bars are SD. *, p≦0.005; **, p≦0.001.

FIGS. 3G-H. Loss of CD drives mesenchymal transformation of GBM. 3 g, Immunofluorescence staining for βIII-tubulin (upper panels) and PSD95 (lower panels) in glioma cells expressing δ-catenin or the empty vector. 3 h, Western blot using the indicated antibodies in glioma cells expressing δ-catenin or the empty vector. Vinculin is shown as control for loading.

FIG. 4A. EGFR-SEPT14 gene fusion identified by whole transcriptome sequencing. Split reads are shown aligning on the breakpoint. The predicted reading frame at the breakpoint is shown at the top with EGFR sequences in blue and SEPT14 in red. The amino acid sequence (TOP) is SEQ ID NO: 1; the nucleotide sequence (bottom) is SEQ ID NO: 2.

FIG. 4B. EGFR-SEPT14 gene fusion identified by whole transcriptome sequencing. (left panel), EGFR-SEPT14-specific PCR from cDNA derived from GBMs. Marker, 1 kb ladder. (right panel), Sanger sequencing chromatogram showing the reading frame at the breakpoint (SEQ ID NO: 4) and putative translation of the fusion protein (SEQ ID NO: 3) in the positive sample.

FIG. 4C. EGFR-SEPT14 gene fusion identified by whole transcriptome sequencing. EGFR-Septin14 fusion protein sequence (SEQ ID NO: 5) and schematics. Regions corresponding to EGFR and Septin14 are shown in blue (left hand side of diagram; (grey in black and white image; sequence comprising “MRP . . . VIQ” amino acids of SEQ ID NO: 5) and red (right hand side of diagram; light grey in black and white image; sequence comprising “LQD . . . RKK” amino acids of SEQ ID NO: 5), respectively. The fusion joins the tyrosine kinase domain of EGFR and the Coiled-coil domain of Septin14.

FIG. 4D. EGFR-SEPT14 gene fusion identified by whole transcriptome sequencing. Genomic fusion of EGFR exon 25 with intron 9 of SEPT14. In the fuse mRNA exon 24 of EGFR is spliced 5′ to exon 10 of SEPT14. Solid arrows indicate the position of the fusion genome primers that generate a fusion specific PCR product in the GBM sample TCGA-27-1837.

FIG. 5A. Expression of EGFR-SEPT14 fusion promotes an aggressive phenotype and inhibition of EGFR kinase delays GBM growth in vivo. Growth rate of SNB19 glioma cells transduced with a lentivirus expressing EGFR-SEPT14, EGFR Viii, EGFR WT or the empty vector (average of triplicate cultures).

FIG. 5B. Expression of EGFR-SEPT14 fusion promotes an aggressive phenotype and inhibition of EGFR kinase delays GBM growth in vivo. Migration assay in SNB19 glioma cells transduced with a lentivirus expressing EGFR-SEPT14, EGFR Viii, EGFR WT or the empty vector.

FIG. 5C. Expression of EGFR-SEPT14 fusion promotes an aggressive phenotype and inhibition of EGFR kinase delays GBM growth in vivo. Quantification of the cell covered area for the experiments shown in b (average of triplicate cultures). All error bars are SD.

FIG. 5D. Expression of EGFR-SEPT14 fusion promotes an aggressive phenotype and inhibition of EGFR kinase delays GBM growth in vivo. In vivo inhibition of tumor growth by EGFR kinase inhibitors in glioma patient derived xenografts carrying EGFR-SEPT14 fusion but not wild type EGFR. T-C indicates the median difference in survival between drug treated and vehicle (control) treated mice.

FIG. 5E. Expression of EGFR-SEPT14 fusion promotes an aggressive phenotype and inhibition of EGFR kinase delays GBM growth in vivo. Kinetics of tumor growth for the same xenografts treated with Lapatinib or vehicle (control). All error bars are SD.

FIG. 6 shows the distribution of substitutions from whole exome data.

FIG. 7. shows dinucleotide distribution in mutated sites.

FIG. 8. Sequence alignment of selected LZTR-1 orthologs. Mutations detected in GBM are indicated in red above of the aligned sequences. The LZTR-1 gene is present in most metazoans, including the sponge Amphimedon queenslandica, which is generally recognized as the most ancient surviving metazoan lineage¹⁷. LZTR-1 is also present in some near-metazoan unicellular protists, including Capsaspora owczarzaki (included in the Figure) and the choanoflagellates Salpingoeca rosetta and Monosiga brevicollis. These opisthokonts are key organisms for the study of the evolution of multicellularity, differentiation and cell-cell communication in animals and help in our understanding of the role of molecular pathways in cancer¹⁸. LZTR-1 has a characteristic Kelch-BTB-BACK-BTB-BACK domain architecture, and unlike the BTB-BACK-Kelch proteins⁸, there has been little, if any, duplication of the LZTR-1 gene since its appearance. Despite its name, LZTR-1 does not contain a leucine zipper region. Figure discloses SEQ ID NOS 8479-8482, respectively, in order of appearance.

FIG. 9. Sequence alignment of BTB-BACK domains. The two BTB-BACK domains of LZTR-1 are included along with the predicted secondary structure from HHpred⁶. The 3-box is the Cul3 binding element within the BACK domain. The secondary structure of KLHL3 (PDB ID 4HXI), KLHL11 (PDB ID 4AP2) and Gigaxonin (PDB ID 3HVE) are based on the crystal structures. The secondary structure of SPOP is based on a crystal structure for the BTB and 3-box region (PDB ID 3HTM) and HHpred predictions from the remainder of the BACK domain. Only the N-terminal half of the BACK domain from KLHL3, KLHL11 and Gigaxonin is included, as SPOP and LZTR-1 contain truncated versions of the BACK domain. Figure discloses SEQ ID NOS 8483-8488, respectively, in order of appearance.

FIG. 10A. Pattern of somatic mutations, CNVs and expression of CTNND2 in GBM. Schematic representation of identified somatic mutations in CTNND2 shown in the context of the known domain structure of the protein. Numbers refer to amino acid residues of the δ-catenin protein.

FIG. 10B. Pattern of somatic mutations, CNVs and expression of CTNND2 in GBM. Somatic deletions of CTNND2. Samples are sorted according to the focality of CTNND2 deletion. In the red-blue scale, white corresponds to normal (diploid) copy number, blue is deletion and red is gain.

FIG. 10C. Pattern of somatic mutations, CNVs and expression of CTNND2 in GBM. Pattern of expression of δ-catenin in the developing mouse brain (embryonic day 14.5), as determined by immunostaining. The highest levels of δ-catenin are detected in the cortical plate (CP) that contains differentiating neurons. IZ, intermediate zone; VZ/SVZ ventricular zone/subventricular zone; LV, lateral ventricle.

FIG. 10D. Pattern of somatic mutations, CNVs and expression of CTNND2 in GBM. CTNND2 mRNA expression analysis from Atlas-TCGA samples shows that CTNND2 is significantly down-regulated in the mesenchymal subgroup. In the green-red scale, black is the median, green is down-regulation and red is up-regulation.

FIG. 11A. EGFR-PSPH gene fusion identified by whole transcriptome sequencing. Split reads are shown aligning on the breakpoint. The predicted reading frame at the breakpoint is shown at the top with EGFR sequences in blue (grey in black and white image; encompassing “SRR . . . VIQ” amino acids and “AGT . . . CAG” nucleotides) and PSPH in red (light grey in black and white image; encompassing “DAF . . . QQV” amino acids and “GAT . . . CAA” nucleotides). The amino acid sequence (TOP) is SEQ ID NO: 7; the nucleotide sequence (bottom) is SEQ ID NO: 8.

FIG. 11B. EGFR-PSPH gene fusion identified by whole transcriptome sequencing. (left panel), EGFR-PSHP specific PCR from cDNA derived from GBMs. Marker, 1 kb ladder. (right panel), Sanger sequencing chromatogram showing the reading frame (SEQ ID NO: 10) at the breakpoint and putative translation of the fusion protein (SEQ ID NO: 9) in the positive sample.

FIG. 11C. EGFR-PSPH gene fusion identified by whole transcriptome sequencing. EGFR-PSPH fusion protein sequence (SEQ ID NO: 11) and schematics. Regions corresponding to EGFR and PSPH are shown in blue (grey in black and white image; left hand side of schematic; sequence comprising “MRP . . . VIQ” amino acids of SEQ ID NO: 11) and red (light grey in black and white image; right hand side of schematic, encompassing amino acids “DAF . . . LEE” of SEQ ID NO: 11), respectively. The fusion includes the tyrosine kinase domain of EGFR and the last 35 amino acids of PSPH.

FIG. 12A. NFASC-NTRK1 gene fusion identified by whole transcriptome sequencing. Split reads are shown aligning on the breakpoint. The predicted reading frame at the breakpoint is shown at the top with NFASC sequences in blue (grey in black and white image; encompassing “RVQ . . . GED” amino acids and “AGA . . . ATT” nucleotides) and NTRK1 in red (light grey in black and white image; encompassing “YTN . . . VGL” amino acids and “AGA . . . AAG” nucleotides). Figure discloses SEQ ID NOS 8489-8490, respectively, in order of appearance.

FIG. 12B. NFASC-NTRK1 gene fusion identified by whole transcriptome sequencing. (left panel), NFASC-NTRK1 specific PCR from cDNA derived from GBMs. Marker, 1 kb ladder. (right panel), Sanger sequencing chromatogram showing the reading frame (SEQ ID NO: 8491) at the breakpoint and putative translation of the fusion protein (SEQ ID NO: 8492) in the positive sample.

FIG. 12C. NFASC-NTRK1 gene fusion identified by whole transcriptome sequencing. NFASC-NTRK1 fusion protein sequence (SEQ ID NO: 8493) and schematics. Regions corresponding to NFASC and NTRK1 are shown in blue (grey in black and white image; sequence comprising “MAR . . . GED” amino acids) and red (light grey in black and white image; sequence comprising “YTN . . . VLG” amino acids), respectively. The fusion includes two of the five fibronectin-type III domain of neurofascin and the protein kinase domain of NTRK1.

FIG. 12D. NFASC-NTRK1 gene fusion identified by whole transcriptome sequencing. Genomic fusion of NFASC intron 9 with intron 21 of NTRKJ. In the fuse mRNA exon 21 of NFASC is spliced 5′ to exon 10 of NTRKJ. Solid arrows indicate the position of the fusion genome primers that generate a fusion specific PCR product in the GBM sample TCGA-06-5411.

FIG. 13 shows the expression measured by read depth from RNA-seq data. Note the very high level of expression in the regions of the genes implicated in the fusion events.

FIG. 14A. CAND1-EGFR gene fusion identified by whole transcriptome sequencing. Split reads are shown aligning on the breakpoint. The predicted reading frame at the breakpoint is shown at the top with CAND1 sequences in blue (grey in black and white image; sequence comprising “TSA . . . LSR” amino acids of SEQ ID NO: 13 and “TTA . . . CAG” nucleotides of SEQ ID NO: 14) and EGFR in red (light grey in black and white image; sequence comprising “CTG . . . VGX” amino acids of SEQ ID NO: 13 and “ATC . . . GGC” nucleotides of SEQ ID NO: 14). The amino acid sequence (TOP) is SEQ ID NO: 13; the nucleotide sequence (bottom) is SEQ ID NO: 14.

FIG. 14B. CAND1-EGFR gene fusion identified by whole transcriptome sequencing. (left panel), CAND1-EGFR specific PCR from cDNA derived from GBMs. Marker, 1 kb ladder. (right panel), Sanger sequencing chromatogram showing the reading frame at the breakpoint (SEQ ID NO: 15) and putative translation of the fusion protein (SEQ ID NO: 16) in the positive sample (boxed sequences). Figure also discloses SEQ ID NO: 8494.

FIG. 14C. CAND1-EGFR gene fusion identified by whole transcriptome sequencing. CAND1-EGFR fusion protein sequence (SEQ ID NO: 8495). Regions corresponding to CAND1 and EGFR are shown in blue (grey in black and white image; sequence comprising “MAS . . . LSR” amino acids of SEQ ID NO: 8495) and red (grey in black and white image; sequence comprising “CTG . . . IGA*” amino acids of SEQ ID NO: 8495), respectively.

FIG. 14D. CAND1-EGFR gene fusion identified by whole transcriptome sequencing. Genomic fusion of CAND1 intron 4 with intron 15 of EGFR. In the fuse mRNA exon 4 of CAND1 is spliced 5′ to exon 16 of EGFR.

FIG. 15 is a photographic image of a blot showing the interaction with Cul3 and protein stability of wild type and mutant LZTR-1. Lysates from SF188 glioma cells transfected with vectors expressing Myc-LZTR-1 and Flag-Cul3 or the empty vector were immunoprecipitated with Flag antibody and assayed by western blot with the indicated antibodies. *, non specific band; arrowhead indicates neddylated Cul3.

FIG. 16A are a photographic images of a blot showing the interaction with Cul3 and protein stability of wild type and mutant LZTR-1. In vitro analysis of the interaction between Cul3 and LZTR-1 wild type and GBM related mutants. Left panel, In vitro translated Myc-LZTR-1 input. Right panel, In vitro translated Myc-LZTR-1 was mixed with Flag-Cul3 immunoprecipitated from transfected HEK-293T cells. Bound proteins were analyzed by western blot using the indicated antibodies.

FIG. 16B is a photographic image of a blot showing the interaction with Cul3 and protein stability of wild type and mutant LZTR-1. Steady state protein levels of wild type LZTR-1 and GBM-related mutants.

FIG. 16C is a photographic image of a blot (top) and a graph (bottom) Top panel, Cells transfected with LZTR-1 wild type or the R810W mutant were treated with cycloexamide for the indicated time. Bottom panel, Quantification of LZTR-1 wild type and LZTR-1-R810W protein from the experiment in the left panel.

FIG. 16D is a photographic image of a blot showing the interaction with Cul3 and protein stability of wild type and mutant LZTR-1. Semi-quantitative RT-PCR evaluation of LZTR-1 wild type and LZTR-1-R810W RNA expression in cells transfected as in FIG. 16C.

FIG. 17A is a graph showing functional analysis of LZTR-1 wild type and GBM associated mutants in GBM-derived cells. GSEA shows up-regulation of genes associated with the phenotype of “spherical cultures” of glioma cells in primary human GBM carrying mutations in the LZTR-1 gene [Enrichment Score (ES)=0.754; P (family-wise error rate, FWER)=0.000 q (false discovery rate, FDR)=0.000].

FIG. 17B is a graph showing functional analysis of LZTR-1 wild type and GBM associated mutants in GBM-derived cells. Sphere forming assay (left panel) and western blot analysis (right panel) of GBM-derived glioma spheres (#48) expressing vector or LZTR-1. Data are Mean±SD of triplicate samples (p=0.0036). Error bars are SD.

FIG. 17C is a linear regression plot of in vitro limiting dilution assay using GBM-derived glioma spheres #46 expressing vector or LZTR-1. The frequency of sphere forming cells was 8.49±1.04 and 1.44±0.05% in vector and LZTR-1 expressing cells, respectively (p=0.00795). Each data point represents the average of triplicates. Error bars are SD.

FIG. 17D is a graph and photographic microscopy images showing functional analysis of LZTR-1 wild type and GBM associated mutants in GBM-derived cells. Left upper panels, Bright field microphotographs of GBM-derived line 46 cells six days after transduction with vector or LZTR-1 expressing lentivirus. Left lower panels, Bright field microphotographs of spheres from GBM-derived glioma cells #46 expressing lentivirus expressing vector or LZTR-1 from experiment in FIG. 17C. Right panel, The size of tumor spheres from cultures in c was determined by microscopy review after 14 days of culture. n=60 spheres from triplicates for each condition. Data are Mean±SD (p<0.0001). Error bars are SD.

FIG. 17E is a photographic image of a western blot analysis of GBM-derived cells #84 expressing vector or LZTR-1.

FIG. 17F is a linear regression plot of in vitro limiting dilution assay using GBM-derived line 84 expressing vector, LZTR-1, LZTR-1-R810W or LZTR-1-W437STOP. The frequency of sphere forming cells was 7.2±0.92 for vector, 1.48±0.09 for LZTR-1 wild type (p=0.0096); 7.82±0.99 for LZTR-1-R810W (p=0.2489); and 6.74±1.07 for LZTR-1-W437STOP (p=0.2269). Error bars are SD.

FIGS. 18A-B are photographic microscopy images showing expression of δ-catenin in neurons and δ-catenin driven loss of mesenchymal marker in GBM. FIG. 18A shows a pattern of expression of δ-catenin in the developing brain, as determined by immunostaining. Double immunofluorescence staining of brain cortex using δ-catenin antibody (red; dark grey in black and white image (center)) and βIII-tubulin (green; light grey in black and white image (right)); Nuclei are counterstained with Dapi (blue; grey in black and white image (Left)). FIG. 18B shows a pattern of expression of δ-catenin in the adult brain, as determined by immunostaining. Upper panels, Double immunofluorescence staining of brain cortex using δ-catenin antibody (red; dark grey in black and white image (center)) and MAP2 (green; light grey in black and white image (right)); Nuclei are counterstained with Dapi (blue; grey in black and white image (Left)). Lower panels, Double immunofluorescence staining of brain cortex using δ-catenin antibody (red; dark grey in black and white image) and GFAP (green; light grey in black and white image); Nuclei are counterstained with Dapi (blue; grey in black and white image).

FIG. 18C is a photographic image of a western blot using the indicated antibodies for U87 cells expressing δ-catenin wild type, glioma-associated δ-catenin mutants or the empty vector. FBN, fibronectin. Vinculin is shown as control for loading.

FIGS. 19A-B show a functional analysis of δ-catenin in mesenchymal GBM. FIG. 19A is a photographic microscopy image of immunofluorescence for fibronectin, collagen-5α1 (COL5A1) and smooth muscle actin (SMA) in glioma spheres #48 four days after infection with lentiviruses expressing δ-catenin or the empty vector. Nuclei are counterstained with Dapi. FIG. 19B is a bar graph showing the quantification of fluorescence intensity for SMA, COL5A1 and FBN for cultures treated as in a. n=3 independent experiments; data indicate mean±SD.

FIG. 19C is a bar graph showing the quantification of fluorescence intensity for βIII-tubulin in cells #48 infected with lentiviruses expressing CTNND2 or the empty vector.

FIG. 19D are photographic microscopy images showing time course analysis of βIII-tubulin expression in glioma spheres #48 transduced with lentiviruses expressing CTNND2 or the empty vector. Note the loss from the advanced culture of βIII-Tubulin expressing cells.

FIGS. 19E-F are graphs. FIG. 19E shows a linear regression plot of in vitro limiting dilution assay using GBM-derived cells #48 expressing vector or δ-catenin. The frequency of sphere forming cells was 7.42±1.16 and 0.88±0.02 for vector and δ-catenin, respectively (p=0.0098). Error bars are SD. FIG. 19F shows a longitudinal analysis of bioluminescence imaging in mice injected intracranially with GBM-derived line 48 expressing vector or δ-catenin. n=3 mice for vector and 5 for δ-catenin. Data are mean±SEM of photon counts.

FIGS. 20A-E show the functional analysis of EGFR-SEPT14 fusion and effect of inhibition of EGFR kinase on glioma growth. FIG. 20A is a graph of a sphere forming assay in the absence of EGF of GBM-derived primary cells (#48) expressing vector, EGFR wild type, EGFR Viii or EGFR-SEP14 fusion. Data are Mean±SD of triplicate samples (p=0.0051 and 0.027 for EGFR-SEP14 fusion and EGFR Viii compared with vector, respectively). FIG. 20B is a western blot analysis of GBM-derived primary cells (#48) expressing vector, EGFR Viii or EGFR-SEP14 fusion cultured in the presence of EGF. FIG. 20C is a photohraphic image of a blot showing GBM-derived cells (#48) expressing vector, EGFR Viii or EGFR-SEP14 fusion that were cultured in the absence of EGF for 48 h and then stimulated with EGF 20 ng/ml for the indicated time. Cells were assayed by western blot using the indicated antibodies. FIG. 20D is a graph of GSEA showing up-regulation of STAT3 target genes in primary human GBM carrying the EGFR-SEPT14 fusion gene [Enrichment Score (ES)=0.738; P (family-wise error rate, FWER)=0.000 q (false discovery rate, FDR)=0.000]. FIG. 20E is a bar graph showing the survival of GBM-derived cells (#48) expressing vector, EGFR wild type, EGFR Viii or EGFR-SEP14 fusion after treatment with lapatinib for 48 h at the indicated concentrations. Data are Mean±SD of triplicate samples.

FIG. 21 is a plot showing the number of mutations in TCGA samples harboring MutComFocal gene candidates. For a given gene G, the number of mutations M8 was plotted in samples harboring G as solid circles. The mean of M8 is also plotted as asterisks. Given the mean, t and standard deviation σ of the number of mutations in all TCGA samples, the 95% confidence interval of a sample being hyper-mutated (11±1.96*a) was plotted and shown that for all G, the mean of M8 falls well within the 95% confidence interval, demonstrating that MutComFocal genes do not tend to occur in hypermutated samples.

FIGS. 22A-B show pattern of somatic mutations, CNVs and expression of CTNND2 in GBM. FIG. 22A are photograpgic microscopy images of immunofluorescence staining of human primary GBM included in tissue microarrays (TMA) using δ-catenin antibody (red; darkt grey in black and white image); Nuclei are counterstained with Dapi (blue; grey in black and white image). Two representative δ-catenin-positive and two δ-catenin-negative tumors are shown in the upper and lower panels, respectively. FIG. 22B is a Western Blot analysis of the expression of δ-catenin in a panel of GBM-derived glioma sphere cultures. Brain, normal human brain. Arrowhead indicated δ-catenin; Asterisk, non-specific band. Vinculin is shown as control for loading.

FIGS. 23A-B show the effects of expression of δ-catenin in glioma cells. FIG. 23A is a western blot using the indicated antibodies in glioma cells expressing δ-catenin or the empty vector. Vinculin is shown as control for loading. FIG. 23B are photographic microscopy images showing U87 glioma cells transduced with a lentivirus expressing wild type δ-catenin, δ-catenin GBM-derived mutants or the empty vector were analyzed by fluorescence microscopy.

FIG. 23C is a bar graph that shows the effects of expression of δ-catenin in glioma cells. The number of cells displaying neural processes was scored. At least 200 cells/sample were analyzed.

FIG. 23D are photographs of longitudinal bioluminescence imaging for one representative mouse injected intracranially with glioma sphere cells #48 transduced with lentivirus expressing CTNND2 (lower panels) or the empty vector (upper panels).

FIG. 24 is a heat map showing amplification surrounding the genomic neighborhood of EGFR, SEPT14, and PSPH among samples harboring EGFR fusions. Copy number was plotted log 2 ratio across the genomic region of chr7:55000000-56500000 for samples with EGFR-PSPH (top three rows) and EGFR-SEPT14 (bottom six rows). Genomic coordinates are also plotted for EGFR (blue; dark grey in black and white image), SEPT14 (yellow; light grey in black and white image), and PSPH (cyan; grey in black and white image).

FIG. 25 is a plot showing the expression of EGFR-SEPT14 fusion promotes an aggressive phenotype and inhibition of EGFR kinase delays GBM growth in vivo. Growth rate of U87glioma cells transduced with a lentivirus expressing EGFR-SEPT14, EGFR Viii, EGFR WT or the empty vector (average of triplicate cultures).

FIG. 26 is a map showing differential expression of GBM tumor samples harboring EGFR-SEPT14 fusions and EGFRv111 rearrangements. After filtering for statistical significance for differential expression, ten genes remained that characterized the EGFR-SEPT14 phenotype from the EGFRv111 phenotype. Log 2 expression was plotted as a heat map. Samples were hierarchically clustered by Euclidean distance using average linkage. This clustering demonstrates clear separation between EGFR-SEPT14 samples (red; dark grey in black and white image; corresponding to top half of intensity bar of left hand side) and EGFRv111 samples (green; light grey in black and white image; corresponding to bottom half of intensity bar of left hand side), confirming the unique molecular signature of the EGFR-SEPT14 gene fusion.

DETAILED DESCRIPTION OF THE INVENTION

Gene fusions retaining the RTK-coding domain of EGFR are the most frequent gene fusion events in GBM. EGFR gene fusions occur in 7.6% of GBM patients and frequently implicate the Sept14 gene as the 3′ partner in the fusion, with a consistent breakpoint at the RNA level. This makes the EGFR fusions highly manageable genetic alterations both diagnostically and therapeutically. In one embodiment, EGFR fusions enhance the proliferative and migratory capacity of glioma cells. In another embodiment, the EGFR fusions also confer sensitivity to EGFR inhibition to human GBM grown as mouse xenografts. Gene fusions encompassing RTK-coding genes are thus implicated in the pathogenesis of GBM and provide a strong rationale for the inclusion of GBM patients harboring EGFR fusions in clinical trials based on EGFR inhibitors. The target population of GBM patients who may carry EGFR gene fusions can benefit from targeted inhibition of EGFR kinase activity, and is estimated to correspond to 20,000 patients per year world-wide (˜1,000 in USA/year).

Glioblastoma multiformes (GBMs) are the most common form of brain tumors in adults accounting for 12-15% of intracranial tumors and 50-60% of primary brain tumors. GBM is among the most lethal forms of human cancer. The history of successful targeted therapy of cancer largely coincides with the inactivation of recurrent and oncogenic gene fusions in hematological malignancies and recently in some types of epithelial cancer. GBM is among the most lethal and incurable forms of human cancer. Targeted therapies against common genetic alterations in GBM have not changed the dismal clinical outcome of the disease, most likely because they have systematically failed to eradicate the truly addicting oncoprotein activities of GBM. Recurrent chromosomal rearrangements resulting in the creation of oncogenic gene fusions have not been found in GBM.

GBM is among the most difficult forms of cancer to treat in humans (1). So far, the therapeutic approaches that have been tested against potentially important oncogenic targets in GBM have met limited success (2-4). Recurrent chromosomal translocations leading to production of oncogenic fusion proteins are viewed as initiating and addicting events in the pathogenesis of human cancer, thus providing the most desirable molecular targets for cancer therapy (5, 6). Recurrent and oncogenic gene fusions have not been found in GBM. Chromosomal rearrangements are hallmarks of hematological malignancies but recently they have also been uncovered in subsets of solid tumors (breast, prostate, lung and colorectal carcinoma) (7, 8). Important and successful targeted therapeutic interventions for patients whose tumors carry these rearrangements have stemmed from the discovery of functional gene fusions, especially when the translocations involve kinase-coding genes (BCR-ABL, EML4-ALK) (9, 10). GBM, the most common malignant brain tumor, remains one of the most challenging forms of cancer to treat. The abundance of passenger mutations and large regions of copy number alterations has complicated the definition of the landscape of driver mutations in glioblastoma.

A hallmark of GBM is rampant chromosomal instability (CIN), which leads to aneuploidy (11). CIN and aneuploidy are early events in the pathogenesis of cancer (12). Without being bound by theory, genetic alterations targeting mitotic fidelity might be responsible for missegregation of chromosomes during mitosis, resulting in aneuploidy (13, 14).

Epidermal growth factor receptors (EGFR) are transmembrane glycoproteins and members of the protein kinase superfamily. This protein is a receptor for members of the epidermal growth factor family. EGFR is a cell surface protein that binds to epidermal growth factor. Binding of the protein to a ligand induces receptor dimerization and tyrosine autophosphorylation and leads to cell proliferation. Mutations that lead to EGFR overexpression or overactivity have been associated with a number of cancers, including lung cancer, anal cancers and glioblastoma multiforme.

Phosphoserine phosphatase (PSPH) is an enzyme responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome.

The singular forms “a,” “an,” and “the” include plural reference unless the context clearly dictates otherwise.

The term “about” is used herein to mean approximately, in the region of, roughly, or around. When the term “about” is used in conjunction with a numerical range, it modifies that range by extending the boundaries above and below the numerical values set forth. In general, the term “about” is used herein to modify a numerical value above and below the stated value by a variance of 20%.

DNA and AminoAcid Manipulation Methods and Purification Thereof

The practice of aspects of the present invention can employ, unless otherwise indicated, conventional techniques of cell biology, cell culture, molecular biology, transgenic biology, microbiology, recombinant DNA, and immunology, which are within the skill of the art. Such techniques are explained fully in the literature. See, e.g., Molecular Cloning A Laboratory Manual, 3^(rd) Ed., ed. by Sambrook (2001), Fritsch and Maniatis (Cold Spring Harbor Laboratory Press: 1989); DNA Cloning, Volumes I and II (D. N. Glover ed., 1985); Oligonucleotide Synthesis (M. J. Gait ed., 1984); Mullis et al. U.S. Pat. No. 4,683,195; Nucleic Acid Hybridization (B. D. Hames & S. J. Higgins eds. 1984); Transcription and Translation (B. D. Hames & S. J. Higgins eds. 1984); Culture Of Animal Cells (R. I. Freshney, Alan R. Liss, Inc., 1987); Immobilized Cells and Enzymes (IRL Press, 1986); B. Perbal, A Practical Guide To Molecular Cloning (1984); the series, Methods In Enzymology (Academic Press, Inc., N.Y.), specifically, Methods In Enzymology, Vols. 154 and 155 (Wu et al. eds.); Gene Transfer Vectors For Mammalian Cells (J. H. Miller and M. P. Calos eds., 1987, Cold Spring Harbor Laboratory); Immunochemical Methods In Cell And Molecular Biology (Caner and Walker, eds., Academic Press, London, 1987); Handbook Of Experimental Immunology, Volumes I-IV (D. M. Weir and C. C. Blackwell, eds., 1986); Manipulating the Mouse Embryo, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). All patents, patent applications and references cited herein are incorporated by reference in their entireties.

One skilled in the art can obtain a protein in several ways, which include, but are not limited to, isolating the protein via biochemical means or expressing a nucleotide sequence encoding the protein of interest by genetic engineering methods.

A protein is encoded by a nucleic acid (including, for example, genomic DNA, complementary DNA (cDNA), synthetic DNA, as well as any form of corresponding RNA). For example, it can be encoded by a recombinant nucleic acid of a gene. The proteins of the invention can be obtained from various sources and can be produced according to various techniques known in the art. For example, a nucleic acid that encodes a protein can be obtained by screening DNA libraries, or by amplification from a natural source. A protein can be a fragment or portion thereof. The nucleic acids encoding a protein can be produced via recombinant DNA technology and such recombinant nucleic acids can be prepared by conventional techniques, including chemical synthesis, genetic engineering, enzymatic techniques, or a combination thereof. For example, a fusion protein of the invention comprises a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. For example, the fusion protein can be an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND fusion protein. An example of an EGFR-SEPT fusion protein is EGFR-SEPT14. In one embodiment, an EGFR-SEPT14 fusion polypeptide can have the amino acid sequence shown in SEQ ID NO: 1, 3, or 5. An example of an EGFR-PSPH fusion protein is a polypeptide having the amino acid sequence shown in SEQ ID NO: 7, 9, or 11. An example of an EGFR-CAND fusion protein is EGFR-CAND1. In one embodiment, an EGFR-CAND1 fusion polypeptide can have the amino acid sequence shown in SEQ ID NO: 13, 16, or 8495.

The Genbank ID for the EGFR gene is 1956. Four isoforms are listed for EGFR, e.g., having Genebank Accession Nos. NP_005219 (corresponding nucleotide sequence NM_005228); NP_958439 (corresponding nucleotide sequence NM_201282); NP_958440 (corresponding nucleotide sequence NM_201283); NP_958441 (corresponding nucleotide sequence NM_201284). The nucleotide and amino acid sequences can be readily obtained by one of ordinary skill in the art using the listed accession numbers.

The Genbank ID for the SEPT14 gene is 346288. The Genebank Accession No. for SEPT14 is NP_997249 (corresponding nucleotide sequence NM_207366). The nucleotide and amino acid sequences can be readily obtained by one of ordinary skill in the art using the listed accession numbers.

The Genbank ID for the PSPH gene is 5723. The Genebank Accession No. for PSPH is NP_004568 (corresponding nucleotide sequence NM_004577). The nucleotide and amino acid sequences can be readily obtained by one of ordinary skill in the art using the listed accession numbers.

The Genbank ID for the CAND1 gene is 55832. The Genebank Accession No. for CAND1 is NP_060918 (corresponding nucleotide sequence NM_018448). The nucleotide and amino acid sequences can be readily obtained by one of ordinary skill in the art using the listed accession numbers.

As used herein, an “EGFR fusion molecule” can be a nucleic acid which encodes a polypeptide corresponding to a fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. For example, an EGFR fusion molecule can include an EGFR-SEPT fusion (e.g., an EGFR-SEPT14 fusion polypeptide comprising the amino acid sequence shown in SEQ ID NO: 1, 3, or 5, or comprising the nucleic acid sequence shown in SEQ ID NO: 2 or 4); an EGFR-PSPH fusion, (e.g., comprising the amino acid sequence shown in SEQ ID NO: 7, 9, or 11, or comprising the nucleic acid sequence shown in SEQ ID NO: 8 or 10), or an EGFR-CAND fusion (e.g., an EGFR-CAND1 fusion polypeptide comprising the amino acid sequence shown in SEQ ID NO: 13, 16, or 8495, or comprising the nucleic acid sequence shown in SEQ ID NO: 14 or 15). For example, an EGFR fusion molecule can include an EGFR-containing fusion comprising the amino acid sequence corresponding to Genebank Accession no. NP_005219, NP_958439, NP_958440, or NP_958441. AN EGFR fusion molecule can also include a tyrosine kinase domain of an EGFR protein fused to a protein encoded by any one of the genes listed in Table 10. AN EGFR fusion molecule can include a variant of the above described examples, such as a fragment thereof

TABLE 10 Fusion Partners gene gene gene gene ABCA13 C21orf29 CAMKK1 DNAJC6 ABCC1 CACNA1C CAMSAP1 DYRK3 ABCC12 CACNA1G CAMTA1 EIF2C2 ABCC6 CNTNAP4 CAP2 FAM184B ABL1 CUL3 CCDC147 FREM2 ADAM12 DMD CCDC158 GDPD2 ADCY10 DUSP27 CELF2 GLI3 ADCY2 ECE1 CILP IL1RN ADCY8 EYS CMYA5 ISX AGBL4 FAM172A COL14A1 KIDINS220 AHNAK FAM184B CORO7 LRBA ANXA7 EGFR4 CSMD2 LY75 AP4S1 ITGAV CUL3 MDH2 AQP2 LRP1 DDI2 MMP12 ARMC6 LY75 DEPDC5 N4BP2L2 ATP5B MAPKAP1 DEPDC7 NCF2 ATP6AP1L MYT1 DI10L NCOR1 ATP6V0D2 NCF2 DMD NCRNA00157 ATXN1 NCOR1 EDA NRXN3 BAHD1 NHSL2 EFHC1 PARP16 BBX NKAIN2 EFS PLA2G2F BCA10 NR3C1 EIF2C2 PLEK2 C15orf23 NUP188 ENTPD2 PRKCH C15orf33 OSBPL10 EYS PTPRS C21orf29 PACSIN1 FAM160A1 ROBO1 C2CD3 PARP16 MUSK SASH3 C6orf170 PDZRN4 NEUROG1 SH3BP5 C7orf44 POLM NHSL2 SLC44A2 CACNA1C PPP1R3A NR3C1 SLC5A4 CACNA1G PSEN1 ODZ1 SNX5 FAM168A PTPRD PCDH12 SORCS2 FAM172A PTPRS PLCL1 SRRM1 FAM192A RALYL PLEKHM3 SSX3 FAM19A2 RERE PLOD3 STAG2 FBXL4 RIMBP2 PRKCH STK24 FH RNF216 PSEN1 SURF6 FREM2 SDAD1 SEPT5 SYNPO2 GAPVD1 SEC14L3 SLC44A2 TAF1 GLI3 SH3RF3 SNTA1 TMEM80 GPR182 SLC9A1 USP48 TNFRSF10B GSTA3 SMOC2 VSNL1 TTYH1 IGFBP3 SNX5 WDFY1 UNC93B1 ITGA9 TACC2 WISP2 VSNL1 ITGB2 SRGAP1 XRRA1 XRCC4 JOSD2 SSX3 LRRC4B ZNF410 KIDINS220 SUMF1 LRRK2 TRIOBP LAMA2 SYNPO2 MAPKAP1 TTYH1 LCLAT1 TNFRSF10B MST1R LRBA LIN9

The nucleic acid can be any type of nucleic acid, including genomic DNA, complementary DNA (cDNA), recombinant DNA, synthetic or semi-synthetic DNA, as well as any form of corresponding RNA. A cDNA is a form of DNA artificially synthesized from a messenger RNA template and is used to produce gene clones. A synthetic DNA is free of modifications that can be found in cellular nucleic acids and include, but are not limited to, histones and methylation. For example, a nucleic acid encoding anan EGFR EGFR fusion molecule can comprise a recombinant nucleic acid encoding such a protein. The nucleic acid can be a non-naturally occurring nucleic acid created artificially (such as by assembling, cutting, ligating or amplifying sequences). It can be double-stranded or single-stranded.

The invention further provides for nucleic acids that are complementary to an EGFR fusion molecule. Complementary nucleic acids can hybridize to the nucleic acid sequence described above under stringent hybridization conditions. Non-limiting examples of stringent hybridization conditions include temperatures above 30° C., above 35° C., in excess of 42° C., and/or salinity of less than about 500 mM, or less than 200 mM. Hybridization conditions can be adjusted by the skilled artisan via modifying the temperature, salinity and/or the concentration of other reagents such as SDS or SSC.

According to the invention, protein variants can include amino acid sequence modifications. For example, amino acid sequence modifications fall into one or more of three classes: substitutional, insertional or deletional variants. Insertions can include amino and/or carboxyl terminal fusions as well as intrasequence insertions of single or multiple amino acid residues. Insertions ordinarily will be smaller insertions than those of amino or carboxyl terminal fusions, for example, on the order of one to four residues. Deletions are characterized by the removal of one or more amino acid residues from the protein sequence. These variants ordinarily are prepared by site-specific mutagenesis of nucleotides in the DNA encoding the protein, thereby producing DNA encoding the variant, and thereafter expressing the DNA in recombinant cell culture.

In one embodiment, an EGFR fusion molecule comprises a protein or polypeptide encoded by a nucleic acid sequence encoding an EGFR fusion molecule, such as the sequences shown in SEQ ID NOS: 2, 4, 8, 10, 14, or 15. In some embodiments, the nuceleic acid sequence encoding an EGFR fusion molecule is about 70%, about 75%, about 80%, about 85%, about 90%, about 93%, about 95%, about 97%, about 98%, or about 99% identical to SEQ ID NOS: 2, 4, 8, 10, 14, or 15. In another embodiment, the polypeptide can be modified, such as by glycosylations and/or acetylations and/or chemical reaction or coupling, and can contain one or several non-natural or synthetic amino acids. An example of an EGFR fusion molecule is the polypeptide having the amino acid sequence shown in SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. In some embodiments, the EGFR fusion molecule that is a polypeptide is about 70%, about 75%, about 80%, about 85%, about 90%, about 93%, about 95%, about 97%, about 98%, or about 99% identical to SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. In another embodiment, an EGFR fusion molecule can be a fragment of an EGFR fusion protein. For example, the EGFR fusion molecule can encompass any portion of at least about 8 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. The fragment can comprise at least about 10 amino acids, a least about 20 amino acids, at least about 30 amino acids, at least about 40 amino acids, at least about 50 amino acids, at least about 60 amino acids, or at least about 75 amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. Fragments include all possible amino acid lengths between about 8 and about 100 amino acids, for example, lengths between about 10 and about 100 amino acids, between about 15 and about 100 amino acids, between about 20 and about 100 amino acids, between about 35 and about 100 amino acids, between about 40 and about 100 amino acids, between about 50 and about 100 amino acids, between about 70 and about 100 amino acids, between about 75 and about 100 amino acids, or between about 80 and about 100 amino acids. Fragments include all possible amino acid lengths between about 100 and 800 amino acids, for example, lengths between about 125 and 800 amino acids, between about 150 and 800 amino acids, between about 175 and 800 amino acids, between about 200 and 800 amino acids, between about 225 and 800 amino acids, between about 250 and 800 amino acids, between about 275 and 800 amino acids, between about 300 and 800 amino acids, between about 325 and 800 amino acids, between about 350 and 800 amino acids, between about 375 and 800 amino acids, between about 400 and 800 amino acids, between about 425 and 800 amino acids, between about 450 and 800 amino acids, between about 475 and 800 amino acids, between about 500 and 800 amino acids, between about 525 and 800 amino acids, between about 550 and 800 amino acids, between about 575 and 800 amino acids, between about 600 and 800 amino acids, between about 625 and 800 amino acids, between about 650 and 800 amino acids, between about 675 and 800 amino acids, between about 700 and 800 amino acids, between about 725 and 800 amino acids, between about 750 and 800 amino acids, or between about 775 and 800 amino acids.

Chemical Synthesis.

Nucleic acid sequences encoding an EGFR fusion molecule can be synthesized, in whole or in part, using chemical methods known in the art. Alternatively, a polypeptide can be produced using chemical methods to synthesize its amino acid sequence, such as by direct peptide synthesis using solid-phase techniques. Protein synthesis can either be performed using manual techniques or by automation. Automated synthesis can be achieved, for example, using Applied Biosystems 431A Peptide Synthesizer (Perkin Elmer).

Optionally, polypeptides fragments can be separately synthesized and combined using chemical methods to produce a full-length molecule. For example, these methods can be utilized to synthesize a fusion protein of the invention. In one embodiment, a fusion protein of the invention comprises a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. For example, the fusion protein can be an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND fusion protein. An example of an EGFR-SEPT fusion protein is EGFR-SEPT14. In one embodiment, an EGFR-SEPT14 fusion polypeptide can have the amino acid sequence shown in SEQ ID NO: 1, 3, or 5. An example of an EGFR-PSPH fusion protein is a polypeptide having the amino acid sequence shown in SEQ ID NO: 7, 9, or 11. An example of an EGFR-CAND fusion protein is EGFR-CAND1. In one embodiment, an EGFR-CAND1 fusion polypeptide can have the amino acid sequence shown in SEQ ID NO: 13, 16, or 8495.

Obtaining, Purifying and Detecting EGFR Fusion Molecules.

A polypeptide encoded by a nucleic acid, such as a nucleic acid encoding an EGFR fusion molecule, or a variant thereof, can be obtained by purification from human cells expressing a protein or polypeptide encoded by such a nucleic acid. Non-limiting purification methods include size exclusion chromatography, ammonium sulfate fractionation, ion exchange chromatography, affinity chromatography, and preparative gel electrophoresis.

A synthetic polypeptide can be substantially purified via high performance liquid chromatography (HPLC), such as ion exchange chromatography (IEX-HPLC). The composition of a synthetic polypeptide, such as an EGFR fusion molecule, can be confirmed by amino acid analysis or sequencing.

Other constructions can also be used to join a nucleic acid sequence encoding a polypeptide/protein of the claimed invention to a nucleotide sequence encoding a polypeptide domain which will facilitate purification of soluble proteins. Such purification facilitating domains include, but are not limited to, metal chelating peptides such as histidine-tryptophan modules that allow purification on immobilized metals, protein A domains that allow purification on immobilized immunoglobulin, and the domain utilized in the FLAGS extension/affinity purification system (Immunex Corp., Seattle, Wash.). Including cleavable linker sequences (i.e., those specific for Factor Xa or enterokinase (Invitrogen, San Diego, Calif.)) between the purification domain and a polypeptide encoded by a nucleic acid of the invention also can be used to facilitate purification. For example, the skilled artisan can use an expression vector encoding 6 histidine residues that precede a thioredoxin or an enterokinase cleavage site in conjunction with a nucleic acid of interest. The histidine residues facilitate purification by immobilized metal ion affinity chromatography, while the enterokinase cleavage site provides a means for purifying the polypeptide encoded by, for example, an EGFR-SEPT, EGFR-CAND, EGFR-PSPH, or EGFR-containing, nucleic acid.

Host cells which contain a nucleic acid encoding an EGFR fusion molecule, and which subsequently express the same, can be identified by various procedures known to those of skill in the art. These procedures include, but are not limited to, DNA-DNA or DNA-RNA hybridizations and protein bioassay or immunoassay techniques which include membrane, solution, or chip-based technologies for the detection and/or quantification of nucleic acid or protein. For example, the presence of a nucleic acid encoding an EGFR fusion molecule can be detected by DNA-DNA or DNA-RNA hybridization or amplification using probes or fragments of nucleic acids encoding the same. In one embodiment, a nucleic acid fragment of an EGFR fusion molecule can encompass any portion of at least about 8 consecutive nucleotides of SEQ ID NOS: 2, 8, or 14. In another embodiment, the fragment can comprise at least about 10 consecutive nucleotides, at least about 15 consecutive nucleotides, at least about 20 conseutive nucleotides, or at least about 30 consecutive nucleotides of SEQ ID NOS: 2, 8, or 14. Fragments can include all possible nucleotide lengths between about 8 and about 100 nucleotides, for example, lengths between about 15 and about 100 nucleotides, or between about 20 and about 100 nucleotides. Nucleic acid amplification-based assays involve the use of oligonucleotides selected from sequences encoding an EGFR fusion molecule nucleic acid, or EGFR fusion molecule nucleic acid to detect transformants which contain a nucleic acid encoding a protein or polypeptide of the same.

Protocols are known in the art for detecting and measuring the expression of a polypeptide encoded by a nucleic acid, such as a nucleic acid encoding an EGFR fusion molecule, using either polyclonal or monoclonal antibodies specific for the polypeptide. Non-limiting examples include enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA), and fluorescence activated cell sorting (FACS). A two-site, monoclonal-based immunoassay using monoclonal antibodies reactive to two non-interfering epitopes on a polypeptide encoded by a nucleic acid, such as a nucleic acid encoding an EGFR fusion molecule, can be used, or a competitive binding assay can be employed.

Labeling and conjugation techniques are known by those skilled in the art and can be used in various nucleic acid and amino acid assays. Methods for producing labeled hybridization or PCR probes for detecting sequences related to nucleic acid sequences encoding a protein, such as EGFR fusion molecule, include, but are not limited to, oligolabeling, nick translation, end-labeling, or PCR amplification using a labeled nucleotide. Alternatively, nucleic acid sequences, such as nucleic acids encoding an EGFR fusion molecule, can be cloned into a vector for the production of an mRNA probe. Such vectors are known in the art, are commercially available, and can be used to synthesize RNA probes in vitro by addition of labeled nucleotides and an appropriate RNA polymerase such as T7, T3, or SP6. These procedures can be conducted using a variety of commercially available kits (Amersham Pharmacia Biotech, Promega, and US Biochemical). Suitable reporter molecules or labels which can be used for ease of detection include radionuclides, enzymes, and fluorescent, chemiluminescent, or chromogenic agents, as well as substrates, cofactors, inhibitors, and/or magnetic particles.

A fragment can be a fragment of a protein, such as an EGFR fusion protein. For example, a fragment of an EGFR fusion can encompass any portion of at least about 8 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. The fragment can comprise at least about 10 consecutive amino acids, at least about 20 consecutive amino acids, at least about 30 consecutive amino acids, at least about 40 consecutive amino acids, a least about 50 consecutive amino acids, at least about 60 consecutive amino acids, at least about 70 consecutive amino acids, at least about 75 consecutive amino acids, at least about 80 consecutive amino acids, at least about 85 consecutive amino acids, at least about 90 consecutive amino acids, at least about 95 consecutive amino acids, at least about 100 consecutive amino acids, at least about 200 consecutive amino acids, at least about 300 consecutive amino acids, at least about 400 consecutive amino acids, at least about 500 consecutive amino acids, at least about 600 consecutive amino acids, at least about 700 consecutive amino acids, or at least about 800 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. Fragments include all possible amino acid lengths between about 8 and 100 about amino acids, for example, lengths between about 10 and about 100 amino acids, between about 15 and about 100 amino acids, between about 20 and about 100 amino acids, between about 35 and about 100 amino acids, between about 40 and about 100 amino acids, between about 50 and about 100 amino acids, between about 70 and about 100 amino acids, between about 75 and about 100 amino acids, or between about 80 and about 100 amino acids.

Cell Transfection

Host cells transformed with a nucleic acid sequence of interest can be cultured under conditions suitable for the expression and recovery of the protein from cell culture. The polypeptide produced by a transformed cell can be secreted or contained intracellularly depending on the sequence and/or the vector used. Expression vectors containing a nucleic acid sequence, such as a nucleic acid encoding an EGFR fusion molecule, can be designed to contain signal sequences which direct secretion of soluble polypeptide molecules encoded by the nucleic acid. Cell transfection and culturing methods are described in more detail below.

A eukaryotic expression vector can be used to transfect cells in order to produce proteins encoded by nucleotide sequences of the vector, e.g. those encoding an EGFR fusion molecule. Mammalian cells can contain an expression vector (for example, one that contains a nucleic acid encoding a fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein) via introducing the expression vector into an appropriate host cell via methods known in the art.

A host cell strain can be chosen for its ability to modulate the expression of the inserted sequences or to process the expressed polypeptide encoded by a nucleic acid, in the desired fashion. Such modifications of the polypeptide include, but are not limited to, acetylation, carboxylation, glycosylation, phosphorylation, lipidation, and acylation. Post-translational processing which cleaves a “prepro” form of the polypeptide also can be used to facilitate correct insertion, folding and/or function. Different host cells which have specific cellular machinery and characteristic mechanisms for post-translational activities (e.g., CHO, HeLa, MDCK, HEK293, and W138), are available from the American Type Culture Collection (ATCC; 10801 University Boulevard, Manassas, Va. 20110-2209) and can be chosen to ensure the correct modification and processing of the foreign protein.

An exogenous nucleic acid can be introduced into a cell via a variety of techniques known in the art, such as lipofection, microinjection, calcium phosphate or calcium chloride precipitation, DEAE-dextran-mediated transfection, or electroporation. Electroporation is carried out at approximate voltage and capacitance to result in entry of the DNA construct(s) into cells of interest (such as glioma cells (cell line SF188), neuroblastoma cells (cell lines IMR-32, SK-N-SH, SH-F and SH-N), astrocytes and the like). Other transfection methods also include modified calcium phosphate precipitation, polybrene precipitation, liposome fusion, and receptor-mediated gene delivery.

Cells that will be genetically engineered can be primary and secondary cells obtained from various tissues, and include cell types which can be maintained and propagated in culture. Non-limiting examples of primary and secondary cells include epithelial cells, neural cells, endothelial cells, glial cells, fibroblasts, muscle cells (such as myoblasts) keratinocytes, formed elements of the blood (e.g., lymphocytes, bone marrow cells), and precursors of these somatic cell types.

Vertebrate tissue can be obtained by methods known to one skilled in the art, such a punch biopsy or other surgical methods of obtaining a tissue source of the primary cell type of interest. In one embodiment, a punch biopsy or removal (e.g., by aspiration) can be used to obtain a source of cancer cells (for example, glioma cells, neuroblastoma cells, and the like). A mixture of primary cells can be obtained from the tissue, using methods readily practiced in the art, such as explanting or enzymatic digestion (for examples using enzymes such as pronase, trypsin, collagenase, elastase dispase, and chymotrypsin). Biopsy methods have also been described in U.S. Pat. No. 7,419,661 and PCT application publication WO 2001/32840, and each are hereby incorporated by reference.

Primary cells can be acquired from the individual to whom the genetically engineered primary or secondary cells are administered. However, primary cells can also be obtained from a donor, other than the recipient, of the same species. The cells can also be obtained from another species (for example, rabbit, cat, mouse, rat, sheep, goat, dog, horse, cow, bird, or pig). Primary cells can also include cells from an isolated or purified vertebrate tissue source grown attached to a tissue culture substrate (for example, flask or dish) or grown in a suspension; cells present in an explant derived from tissue; both of the aforementioned cell types plated for the first time; and cell culture suspensions derived from these plated cells. Secondary cells can be plated primary cells that are removed from the culture substrate and replated, or passaged, in addition to cells from the subsequent passages. Secondary cells can be passaged one or more times. These primary or secondary cells can contain expression vectors having a gene that encodes an EGFR fusion molecule.

Cell Culturing

Various culturing parameters can be used with respect to the host cell being cultured. Appropriate culture conditions for mammalian cells are well known in the art (Cleveland W L, et al., J Immunol Methods, 1983, 56(2): 221-234) or can be determined by the skilled artisan (see, for example, Animal Cell Culture: A Practical Approach 2nd Ed., Rickwood, D. and Hames, B. D., eds. (Oxford University Press: New York, 1992)). Cell culturing conditions can vary according to the type of host cell selected. Commercially available medium can be utilized. Non-limiting examples of medium include, for example, Minimal Essential Medium (MEM, Sigma, St. Louis, Mo.); Dulbecco's Modified Eagles Medium (DMEM, Sigma); Ham's F10 Medium (Sigma); HyClone cell culture medium (HyClone, Logan, Utah); RPMI-1640 Medium (Sigma); and chemically-defined (CD) media, which are formulated for various cell types, e.g., CD-CHO Medium (Invitrogen, Carlsbad, Calif.).

The cell culture media can be supplemented as necessary with supplementary components or ingredients, including optional components, in appropriate concentrations or amounts, as necessary or desired. Cell culture medium solutions provide at least one component from one or more of the following categories: (1) an energy source, usually in the form of a carbohydrate such as glucose; (2) all essential amino acids, and usually the basic set of twenty amino acids plus cysteine; (3) vitamins and/or other organic compounds required at low concentrations; (4) free fatty acids or lipids, for example linoleic acid; and (5) trace elements, where trace elements are defined as inorganic compounds or naturally occurring elements that can be required at very low concentrations, usually in the micromolar range.

The medium also can be supplemented electively with one or more components from any of the following categories: (1) salts, for example, magnesium, calcium, and phosphate; (2) hormones and other growth factors such as, serum, insulin, transferrin, and epidermal growth factor; (3) protein and tissue hydrolysates, for example peptone or peptone mixtures which can be obtained from purified gelatin, plant material, or animal byproducts; (4) nucleosides and bases such as, adenosine, thymidine, and hypoxanthine; (5) buffers, such as HEPES; (6) antibiotics, such as gentamycin or ampicillin; (7) cell protective agents, for example pluronic polyol; and (8) galactose. In one embodiment, soluble factors can be added to the culturing medium.

The mammalian cell culture that can be used with the present invention is prepared in a medium suitable for the type of cell being cultured. In one embodiment, the cell culture medium can be any one of those previously discussed (for example, MEM) that is supplemented with serum from a mammalian source (for example, fetal bovine serum (FBS)). In another embodiment, the medium can be a conditioned medium to sustain the growth of host cells.

Three-dimensional cultures can be formed from agar (such as Gey's Agar), hydrogels (such as matrigel, agarose, and the like; Lee et al., (2004) Biomaterials 25: 2461-2466) or polymers that are cross-linked. These polymers can comprise natural polymers and their derivatives, synthetic polymers and their derivatives, or a combination thereof. Natural polymers can be anionic polymers, cationic polymers, amphipathic polymers, or neutral polymers. Non-limiting examples of anionic polymers can include hyaluronic acid, alginic acid (alginate), carageenan, chondroitin sulfate, dextran sulfate, and pectin. Some examples of cationic polymers, include but are not limited to, chitosan or polylysine. (Peppas et al., (2006) Adv Mater. 18: 1345-60; Hoffman, A. S., (2002) Adv Drug Deliv Rev. 43: 3-12; Hoffman, A. S., (2001) Ann NY Acad Sci 944: 62-73). Examples of amphipathic polymers can include, but are not limited to collagen, gelatin, fibrin, and carboxymethyl chitin. Non-limiting examples of neutral polymers can include dextran, agarose, or pullulan. (Peppas et al., (2006) Adv Mater. 18: 1345-60; Hoffman, A. S., (2002) Adv Drug Deliv Rev. 43: 3-12; Hoffman, A. S., (2001) Ann NY Acad Sci 944: 62-73).

Cells to be cultured can harbor introduced expression vectors, such as plasmids. The expression vector constructs can be introduced via transformation, microinjection, transfection, lipofection, electroporation, or infection. The expression vectors can contain coding sequences, or portions thereof, encoding the proteins for expression and production. Expression vectors containing sequences encoding the produced proteins and polypeptides, as well as the appropriate transcriptional and translational control elements, can be generated using methods well known to and practiced by those skilled in the art. These methods include synthetic techniques, in vitro recombinant DNA techniques, and in vivo genetic recombination which are described in J. Sambrook et al., 2001, Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Press, Plainview, N.Y. and in F. M. Ausubel et al., 1989, Current Protocols in Molecular Biology, John Wiley & Sons, New York, N.Y.

EGFR Fusion Molecule Inhibitors

The invention provides methods for use of compounds that decrease the expression level or activity of an EFGR EGFR fusion molecule in a subject. In addition, the invention provides methods for using compounds for the treatment of a gene-fusion associated cancer. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma.

As used herein, an “EGFR fusion molecule inhibitor” refers to a compound that interacts with an EGFR fusion molecule of the invention and modulates its activity and/or its expression. For example, the compound can decrease the activity or expression of an EGFR fusion molecule. The compound can be an antagonist of an EGFR fusion molecule (e.g., an EGFR fusion molecule inhibitor). Some non-limiting examples of EGFR fusion molecule inhibitors include peptides (such as peptide fragments comprising an EGFR fusion molecule, or antibodies or fragments thereof), small molecules, and nucleic acids (such as siRNA or antisense RNA specific for a nucleic acid comprising an EGFR fusion molecule). Antagonists of an EGFR fusion molecule decrease the amount or the duration of the activity of an EGFR fusion protein. In one embodiment, the fusion protein comprises a tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein (e.g., EGFR-SEPT (such as EFGR-SEPT14), EGFR-PSPH, or EGFR-CAND (such as EGFR-CAND1)). Antagonists include proteins, nucleic acids, antibodies, small molecules, or any other molecule which decrease the activity of an EGFR fusion molecule.

The term “modulate,” as it appears herein, refers to a change in the activity or expression of an EGFR fusion molecule. For example, modulation can cause a decrease in protein activity, binding characteristics, or any other biological, functional, or immunological properties of an EGFR fusion molecule, such as an EGFR fusion protein.

In one embodiment, an EGFR fusion molecule inhibitor can be a peptide fragment of an EGFR fusion protein that binds to the protein itself.

For example, the EGFR fusion polypeptide can encompass any portion of at least about 8 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. The fragment can comprise at least about 10 consecutive amino acids, at least about 20 consecutive amino acids, at least about 30 consecutive amino acids, at least about 40 consecutive amino acids, a least about 50 consecutive amino acids, at least about 60 consecutive amino acids, at least about 70 consecutive amino acids, at least about 75 consecutive amino acids, at least about 80 consecutive amino acids, at least about 85 consecutive amino acids, at least about 90 consecutive amino acids, at least about 95 consecutive amino acids, at least about 100 consecutive amino acids, at least about 200 consecutive amino acids, at least about 300 consecutive amino acids, at least about 400 consecutive amino acids, at least about 500 consecutive amino acids, at least about 600 consecutive amino acids, at least about 700 consecutive amino acids, or at least about 800 consecutive amino acids of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. Fragments include all possible amino acid lengths between about 8 and 100 about amino acids, for example, lengths between about 10 and about 100 amino acids, between about 15 and about 100 amino acids, between about 20 and about 100 amino acids, between about 35 and about 100 amino acids, between about 40 and about 100 amino acids, between about 50 and about 100 amino acids, between about 70 and about 100 amino acids, between about 75 and about 100 amino acids, or between about 80 and about 100 amino acids. These peptide fragments can be obtained commercially or synthesized via liquid phase or solid phase synthesis methods (Atherton et al., (1989) Solid Phase Peptide Synthesis: a Practical Approach. IRL Press, Oxford, England). The EGFR fusion peptide fragments can be isolated from a natural source, genetically engineered, or chemically prepared. These methods are well known in the art.

An EGFR fusion molecule inhibitor can be a protein, such as an antibody (monoclonal, polyclonal, humanized, chimeric, or fully human), or a binding fragment thereof, directed against an EGFR fusion molecule. An antibody fragment can be a form of an antibody other than the full-length form and includes portions or components that exist within full-length antibodies, in addition to antibody fragments that have been engineered. Antibody fragments can include, but are not limited to, single chain Fv (scFv), diabodies, Fv, and (Fab′)₂, triabodies, Fc, Fab, CDR1, CDR2, CDR3, combinations of CDR's, variable regions, tetrabodies, bifunctional hybrid antibodies, framework regions, constant regions, and the like (see, Maynard et al., (2000) Ann. Rev. Biomed. Eng. 2:339-76; Hudson (1998) Curr. Opin. Biotechnol. 9:395-402). Antibodies can be obtained commercially, custom generated, or synthesized against an antigen of interest according to methods established in the art (see U.S. Pat. Nos. 6,914,128, 5,780,597, and 5,811,523; Roland E. Kontermann and Stefan Dübel (editors), Antibody Engineering, Vol. I & II, (2010) 2^(nd) ed., Springer; Antony S. Dimitrov (editor), Therapeutic Antibodies: Methods and Protocols (Methods in Molecular Biology), (2009), Humana Press; Benny Lo (editor) Antibody Engineering: Methods and Protocols (Methods in Molecular Biology), (2004) Humana Press, each of which are hereby incorporated by reference in their entireties). For example, antibodies directed to an EGFR fusion molecule can be obtained commercially from Abcam, Santa Cruz Biotechnology, Abgent, R&D Systems, Novus Biologicals, etc. Human antibodies directed to an EGFR fusion molecule (such as monoclonal, humanized, fully human, or chimeric antibodies) can be useful antibody therapeutics for use in humans. In one embodiment, an antibody or binding fragment thereof is directed against SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495.

Inhibition of RNA encoding an EGFR fusion molecule can effectively modulate the expression of an EGFR fusion molecule Inhibitors are selected from the group comprising: siRNA; interfering RNA or RNAi; dsRNA; RNA Polymerase III transcribed DNAs; ribozymes; and antisense nucleic acids, which can be RNA, DNA, or an artificial nucleic acid.

Antisense oligonucleotides, including antisense DNA, RNA, and DNA/RNA molecules, act to directly block the translation of mRNA by binding to targeted mRNA and preventing protein translation. For example, antisense oligonucleotides of at least about 15 bases and complementary to unique regions of the DNA sequence encoding an EGFR fusion molecule can be synthesized, e.g., by conventional phosphodiester techniques (Dallas et al., (2006) Med. Sci. Monit. 12(4):RA67-74; Kalota et al., (2006) Handb. Exp. Pharmacol. 173:173-96; Lutzelburger et al., (2006) Handb. Exp. Pharmacol. 173:243-59). Antisense nucleotide sequences include, but are not limited to: morpholinos, 2′-O-methyl polynucleotides, DNA, RNA and the like.

siRNA comprises a double stranded structure containing from about 15 to about 50 base pairs, for example from about 21 to about 25 base pairs, and having a nucleotide sequence identical or nearly identical to an expressed target gene or RNA within the cell. The siRNA comprise a sense RNA strand and a complementary antisense RNA strand annealed together by standard Watson-Crick base-pairing interactions. The sense strand comprises a nucleic acid sequence which is substantially identical to a nucleic acid sequence contained within the target miRNA molecule. “Substantially identical” to a target sequence contained within the target mRNA refers to a nucleic acid sequence that differs from the target sequence by about 3% or less. The sense and antisense strands of the siRNA can comprise two complementary, single-stranded RNA molecules, or can comprise a single molecule in which two complementary portions are base-paired and are covalently linked by a single-stranded “hairpin” area. See also, McMnaus and Sharp (2002) Nat Rev Genetics, 3:737-47, and Sen and Blau (2006) FASEB J., 20:1293-99, the entire disclosures of which are herein incorporated by reference.

The siRNA can be altered RNA that differs from naturally-occurring RNA by the addition, deletion, substitution and/or alteration of one or more nucleotides. Such alterations can include addition of non-nucleotide material, such as to the end(s) of the siRNA or to one or more internal nucleotides of the siRNA, or modifications that make the siRNA resistant to nuclease digestion, or the substitution of one or more nucleotides in the siRNA with deoxyribo-nucleotides. One or both strands of the siRNA can also comprise a 3′ overhang. As used herein, a 3′ overhang refers to at least one unpaired nucleotide extending from the 3′-end of a duplexed RNA strand. For example, the siRNA can comprise at least one 3′ overhang of from 1 to about 6 nucleotides (which includes ribonucleotides or deoxyribonucleotides) in length, or from 1 to about 5 nucleotides in length, or from 1 to about 4 nucleotides in length, or from about 2 to about 4 nucleotides in length. For example, each strand of the siRNA can comprise 3′ overhangs of dithymidylic acid (“TT”) or diuridylic acid (“uu”).

siRNA can be produced chemically or biologically, or can be expressed from a recombinant plasmid or viral vector (for example, see U.S. Pat. No. 7,294,504 and U.S. Pat. No. 7,422,896, the entire disclosures of which are herein incorporated by reference). Exemplary methods for producing and testing dsRNA or siRNA molecules are described in U.S. Patent Application Publication No. 2002/0173478 to Gewirtz, U.S. Pat. No. 8,071,559 to Hannon et al., and in U.S. Pat. No. 7,148,342 to Tolentino et al., the entire disclosures of which are herein incorporated by reference.

In one embodiment, an siRNA directed to a human nucleic acid sequence comprising an EGFR fusion molecule can be generated against any one of SEQ ID NOS: 2, 4, 8, 10, 14, or 15. In another embodiment, an siRNA directed to a human nucleic acid sequence comprising a breakpoint of an EGFR fusion molecule can be generated against any one of SEQ ID NOS: 4, 10, or 15.

RNA polymerase III transcribed DNAs contain promoters, such as the U6 promoter. These DNAs can be transcribed to produce small hairpin RNAs in the cell that can function as siRNA or linear RNAs, which can function as antisense RNA. The EGFR fusion molecule inhibitor can comprise ribonucleotides, deoxyribonucleotides, synthetic nucleotides, or any suitable combination such that the target RNA and/or gene is inhibited. In addition, these forms of nucleic acid can be single, double, triple, or quadruple stranded. (See for example Bass (2001) Nature, 411:428-429; Elbashir et al., (2001) Nature, 411:494 498; U.S. Pat. No. 6,509,154; U.S. Patent Application Publication No. 2003/0027783; and PCT Publication Nos. WO 00/044895, WO 99/032619, WO 00/01846, WO 01/029058, WO 00/044914).

EGFR fusion molecule inhibitor can be a small molecule that binds to an EGFR fusion protein described herein and disrupts its function. Small molecules are a diverse group of synthetic and natural substances generally having low molecular weights. They can be isolated from natural sources (for example, plants, fungi, microbes and the like), are obtained commercially and/or available as libraries or collections, or synthesized. Candidate small molecules that inhibit an EGFR fusion protein can be identified via in silico screening or high-through-put (HTP) screening of combinatorial libraries according to methods established in the art (e.g., see Potyrailo et al., (2011) ACS Comb Sci. 13(6):579-633; Mensch et al., (2009) J Pharm Sci. 98(12):4429-68; Schnur (2008) Curr Opin Drug Discov Devel. 11(3):375-80; and Jhoti (2007) Ernst Schering Found Symp Proc. (3):169-85, each of which are hereby incorporated by reference in their entireties.) Most conventional pharmaceuticals, such as aspirin, penicillin, and many chemotherapeutics, are small molecules, can be obtained commercially, can be chemically synthesized, or can be obtained from random or combinatorial libraries as described below (see, e.g., Werner et al., (2006) Brief Funct. Genomic Proteomic 5(1):32-6).

Non-limiting examples of EGFR fusion molecule inhibitors include the EGFR inhibitors AZD4547 (see Gavine et al., (2012) Cancer Res, 72(8); 2045-56; see also PCT Application Publication No. WO2008/075068, each of which are hereby incorporated by reference in their entireties); NVP-BGJ398 (see Guagnano et al., (2011) J. Med. Chem., 54:7066-7083; see also U.S. Patent Application Publication No. 2008-0312248 A1, each of which are hereby incorporated by reference in their entireties); PD173074 (see Guagnano et al., (2011) J. Med. Chem., 54:7066-7083; see also Mohammadi et al., (1998) EMBO J., 17:5896-5904, each of which are hereby incorporated by reference in their entireties); NF449 (EMD Millipore (Billerica, Mass.) Cat. No. 480420; see also Krejci, (2010) the Journal of Biological Chemistry, 285(27):20644-20653, which is hereby incorporated by reference in its entirety); LY2874455 (Active Biochem; see Zhao et al. (2011) Mol Cancer Ther. (11):2200-10; see also PCT Application Publication No. WO 2010129509, each of which are hereby incorporated by reference in their entireties); TKI258 (Dovitinib); BIBF-1120 (Intedanib-Vargatef); BMS-582664 (Brivanib alaninate); AZD-2171 (Cediranib); TSU-68 (Orantinib); AB-1010 (Masitinib); AP-24534 (Ponatinib); and E-7080 (by Eisai). A non-limiting example of an EGFR fusion molecule inhibitor includes the inhibitor KHS101 (Wurdak et al., (2010) PNAS, 107(38): 16542-47, which is hereby incorporated by reference in its entirety).

Structures of EGFR fusion molecule inhibitors useful for the invention include, but are not limited to: the EGFR inhibitor AZD4547,

the EGFR inhibitor NVP-BGJ398,

the EGFR inhibitor PD173074,

the EGFR inhibitor LY2874455

and the EGFR inhibitor NF449 (EMD Millipore (Billerica, Mass.) Cat. No. 480420),

Other EGFR inhibitors include, but are not limited to:

A structure of an EGFR fusion molecule inhibitor useful for the invention includes, but is not limited to the inhibitor KHS101,

Assessment and Therapeutic Treatment

The invention provides a method of decreasing the growth of a solid tumor in a subject. The tumor is associated with, but not limited to glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the method comprises detecting the presence of an EGFR fusion molecule in a sample obtained from a subject. In some embodiments, the sample is incubated with an agent that binds to an EFGR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like. In further embodiments, the method comprises administering to the subject an effective amount of an EGFR fusion molecule inhibitor, wherein the inhibitor decreases the size of the solid tumor.

The invention also provides a method for treating or preventing a gene-fusion associated cancer in a subject, such as, but not limited to, glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the method comprises detecting the presence of an EGFR fusion molecule in a sample obtained from a subject, the presence of the fusion being indicative of a gene-fusion associated cancer, and, administering to the subject in need a therapeutic treatment against a gene-fusion associated cancer. In some embodiments, the sample is incubated with an agent that binds to an EFGR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like.

The invention also provides a method for decreasing in a subject in need thereof the expression level or activity of a fusion protein comprising the tyrosine kinase domain of an EGFR protein fused to a polypeptide that constitutively activates the tyrosine kinase domain of the EGFR protein. In some embodiments, the method comprises obtaining a biological sample from the subject. In some embodiments, the sample is incubated with an agent that binds to an EGFR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like. In some embodiments, the method comprises administering to the subject a therapeutic amount of a composition comprising an admixture of a pharmaceutically acceptable carrier an inhibitor of the fusion protein of the invention. In another embodiment, the method further comprises determining the fusion protein expression level or activity. In another embodiment, the method further comprises detecting whether the fusion protein expression level or activity is decreased as compared to the fusion protein expression level or activity prior to administration of the composition, thereby decreasing the expression level or activity of the fusion protein. In some embodiments, the fusion protein is an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or an EGFR-SEPT fusion protein.

The administering step in each of the claimed methods can comprise a drug administration, such as EGFR fusion molecule inhibitor (for example, a pharmaceutical composition comprising an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND). In one embodiment, the therapeutic molecule to be administered comprises a polypeptide of an EGFR fusion molecule, comprising at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 93%, at least about 95%, at least about 97%, at least about 98%, at least about 99%, or 100% of the amino acid sequence of SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495, and exhibits the function of decreasing expression of such a protein, thus treating a gene fusion-associated cancer. In another embodiment, administration of the therapeutic molecule decreases the size of the solid tumor associated with glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In a further embodiment, administration of the therapeutic molecule decreases cell proliferation in a subject afflicted with a gene-fusion associated cancer.

In another embodiment, the therapeutic molecule to be administered comprises an siRNA directed to a human nucleic acid sequence comprising an EGFR fusion molecule. In one embodiment, the siRNA is directed to any one of SEQ ID NOS: 2, 4, 8, 10, 14, or 15. In a further embodiment, the therapeutic molecule to be administered comprises an antibody or binding fragment thereof, that is directed against SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 16, or 8495. In some embodiments, the therapeutic molecule to be administered comprises a small molecule that specifically binds to an EGFR protein, such as AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, or LY2874455.

An EGFR fusion molecule, for example, a fusion between EGFR and SEPT, PSPH, or CAND, can be determined at the level of the DNA, RNA, or polypeptide. Optionally, detection can be determined by performing an oligonucleotide ligation assay, a confirmation based assay, a hybridization assay, a sequencing assay, an allele-specific amplification assay, a microsequencing assay, a melting curve analysis, a denaturing high performance liquid chromatography (DHPLC) assay (for example, see Jones et al, (2000) Hum Genet., 106(6):663-8), or a combination thereof. In one embodiment, the detection is performed by sequencing all or part of an EGFR fusion molecule (e.g., EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), EGFR-CAND fusion (such as an EGFR-CAND1 fusion), EGFR-PSPH), or by selective hybridization or amplification of all or part of an EGFR fusion molecule (e.g., EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), EGFR-CAND fusion (such as an EGFR-CAND1 fusion), EGFR-PSPH)). AN EGFR fusion molecule specific amplification (e.g., EGFR-SEPT (such as an EGFR-SEPT14), EGFR-CAND (such as an EGFR-CAND1), EGFR-PSPH nucleic acid specific amplification) can be carried out before the fusion identification step.

The invention provides for a method of detecting a chromosomal alteration in a subject afflicted with a gene-fusion associated cancer. In some emboidments, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. In one embodiment, the chromosomal alteration is an in-frame fused transcript described herein, for example an EGFR fusion molecule. An alteration in a chromosome region occupied by an EGFR fusion molecule such as a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH, can be any form of mutation(s), deletion(s), rearrangements) and/or insertions in the coding and/or non-coding region of the locus, alone or in various combination(s). Mutations can include point mutations. Insertions can encompass the addition of one or several residues in a coding or non-coding portion of the gene locus. Insertions can comprise an addition of between 1 and 50 base pairs in the gene locus. Deletions can encompass any region of one, two or more residues in a coding or non-coding portion of the gene locus, such as from two residues up to the entire gene or locus. Deletions can affect smaller regions, such as domains (introns) or repeated sequences or fragments of less than about 50 consecutive base pairs, although larger deletions can occur as well. Rearrangement includes inversion of sequences. The alteration in a chromosome region occupied by an EGFR fusion molecule, e.g., a nucleic acid encoding a an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH, can result in amino acid substitutions, RNA splicing or processing, product instability, the creation of stop codons, production of oncogenic fusion proteins, frame-shift mutations, and/or truncated polypeptide production. The alteration can result in the production of an EGFR fusion molecule, for example, a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion, with altered function, stability, targeting or structure. The alteration can also cause a reduction, or even an increase in protein expression. In one embodiment, the alteration in the chromosome region occupied by an EGFR fusion molecule can comprise a chromosomal rearrangement resulting in the production of an EGFR fusion molecule, such as an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. This alteration can be determined at the level of the DNA, RNA, or polypeptide. In another embodiment, the detection or determination comprises nucleic acid sequencing, selective hybridization, selective amplification, gene expression analysis, or a combination thereof. In another embodiment, the detection or determination comprises protein expression analysis, for example by western blot analysis, ELISA, or other antibody detection methods.

The present invention provides a method for treating a gene-fusion associated cancer in a subject in need thereof. In one embodiment, the method comprises obtaining a sample from the subject to determine the level of expression of an EGFR fusion molecule in the subject. In some embodiments, the sample is incubated with an agent that binds to an EGFR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like. In another embodiment, the detection or determination comprises nucleic acid sequencing, selective hybridization, selective amplification, gene expression analysis, or a combination thereof. In another embodiment, the detection or determination comprises protein expression analysis, for example by western blot analysis, ELISA, or other antibody detection methods. In some embodiments, the method further comprises assessing whether to administer an EGFR fusion molecule inhibitor based on the expression pattern of the subject. In further embodiments, the method comprises administering an EGFR fusion molecule inhibitor to the subject. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma.

In one embodiment, the invention provides for a method of detecting the presence of altered RNA expression of an EFGR fusion molecule in a subject, for example, one afflicted with a gene-fusion associated cancer. In another embodiment, the invention provides for a method of detecting the presence of an EGFR fusion molecule in a subject. In some embodiments, the method comprises obtaining a sample from the subject to determine whether the subject expresses an EGFR fusion molecule. In some embodiments, the sample is incubated with an agent that binds to an EGFR fusion molecule, such as an antibody, a probe, a nucleic acid primer, and the like. In other embodiments, the detection or determination comprises nucleic acid sequencing, selective hybridization, selective amplification, gene expression analysis, or a combination thereof. In another embodiment, the detection or determination comprises protein expression analysis, for example by western blot analysis, ELISA, or other antibody detection methods. In some embodiments, the method further comprises assessing whether to administer an EGFR fusion molecule inhibitor based on the expression pattern of the subject. In further embodiments, the method comprises administering an EGFR fusion molecule inhibitor to the subject. Altered RNA expression includes the presence of an altered RNA sequence, the presence of an altered RNA splicing or processing, or the presence of an altered quantity of RNA. These can be detected by various techniques known in the art, including sequencing all or part of the RNA or by selective hybridization or selective amplification of all or part of the RNA.

In a further embodiment, the method can comprise detecting the presence or expression of an EGFR fusion molecule, such as a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. Altered polypeptide expression includes the presence of an altered polypeptide sequence, the presence of an altered quantity of polypeptide, or the presence of an altered tissue distribution. These can be detected by various techniques known in the art, including by sequencing and/or binding to specific ligands (such as antibodies). In one embodiment, the detecting comprises using a northern blot; real time PCR and primers directed to SEQ ID NOS: 2, 4, 8, 10, 14, or 15; a ribonuclease protection assay; a hybridization, amplification, or sequencing technique to detect an EGFR fusion molecule, such as one comprising SEQ ID NOS: 2, 4, 8, 10, 14, or 15; or a combination thereof. In another embodiment, the PCR primers comprise SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, or 89. In a further embodiment, primers used for the screening of EGFR fusion molecules, comprise SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, or 89. In some embodiments, primers used for genomic detection of an EGFR fusion comprise SEQ ID NOS 40, 41, 42, 43, 44, 45, or 89.

Various techniques known in the art can be used to detect or quantify altered gene or RNA expression or nucleic acid sequences, which include, but are not limited to, hybridization, sequencing, amplification, and/or binding to specific ligands (such as antibodies). Other suitable methods include allele-specific oligonucleotide (ASO), oligonucleotide ligation, allele-specific amplification, Southern blot (for DNAs), Northern blot (for RNAs), single-stranded conformation analysis (SSCA), PFGE, fluorescent in situ hybridization (FISH), gel migration, clamped denaturing gel electrophoresis, denaturing HLPC, melting curve analysis, heteroduplex analysis, RNase protection, chemical or enzymatic mismatch cleavage, ELISA, radio-immunoassays (RIA) and immuno-enzymatic assays (IEMA).

Some of these approaches (such as SSCA and constant gradient gel electrophoresis (CGGE)) are based on a change in electrophoretic mobility of the nucleic acids, as a result of the presence of an altered sequence. According to these techniques, the altered sequence is visualized by a shift in mobility on gels. The fragments can then be sequenced to confirm the alteration. Some other approaches are based on specific hybridization between nucleic acids from the subject and a probe specific for wild type or altered gene or RNA. The probe can be in suspension or immobilized on a substrate. The probe can be labeled to facilitate detection of hybrids. Some of these approaches are suited for assessing a polypeptide sequence or expression level, such as Northern blot, ELISA and RIA. These latter require the use of a ligand specific for the polypeptide, for example, the use of a specific antibody.

Hybridization.

Hybridization detection methods are based on the formation of specific hybrids between complementary nucleic acid sequences that serve to detect nucleic acid sequence alteration(s). A detection technique involves the use of a nucleic acid probe specific for a wild type or altered gene or RNA, followed by the detection of the presence of a hybrid. The probe can be in suspension or immobilized on a substrate or support (for example, as in nucleic acid array or chips technologies). The probe can be labeled to facilitate detection of hybrids. In one embodiment, the probe according to the invention can comprise a nucleic acid directed to SEQ ID NOS: 2, 4, 8, 10, 14, or 15. For example, a sample from the subject can be contacted with a nucleic acid probe specific for a gene encoding an EGFR fusion molecule, and the formation of a hybrid can be subsequently assessed. In one embodiment, the method comprises contacting simultaneously the sample with a set of probes that are specific for an EGFR fusion molecule. Also, various samples from various subjects can be investigated in parallel.

According to the invention, a probe can be a polynucleotide sequence which is complementary to and specifically hybridizes with a, or a target portion of a, gene or RNA corresponding to an EGFR fusion molecule. Useful probes are those that are complementary to the gene, RNA, or target portion thereof. Probes can comprise single-stranded nucleic acids of between 8 to 1000 nucleotides in length, for instance between 10 and 800, between 15 and 700, or between 20 and 500. Longer probes can be used as well. A useful probe of the invention is a single stranded nucleic acid molecule of between 8 to 500 nucleotides in length, which can specifically hybridize to a region of a gene or RNA that corresponds to an EGFR fusion molecule.

The sequence of the probes can be derived from the sequences of the EGFR fusion genes provided herein. Nucleotide substitutions can be performed, as well as chemical modifications of the probe. Such chemical modifications can be accomplished to increase the stability of hybrids (e.g., intercalating groups) or to label the probe. Some examples of labels include, without limitation, radioactivity, fluorescence, luminescence, and enzymatic labeling.

A guide to the hybridization of nucleic acids is found in e.g., Sambrook, ed., Molecular Cloning: A Laboratory Manual (3^(rd) Ed.), Vols. 1-3, Cold Spring Harbor Laboratory, 1989; Current Protocols In Molecular Biology, Ausubel, ed. John Wiley & Sons, Inc., New York, 2001; Laboratory Techniques In Biochemistry And Molecular Biology: Hybridization With Nucleic Acid Probes, Part I. Theory and Nucleic Acid Preparation, Tijssen, ed. Elsevier, N.Y., 1993.

Sequencing.

Sequencing can be carried out using techniques well known in the art, using automatic sequencers. The sequencing can be performed on the complete EGFR fusion molecule or on specific domains thereof.

Amplification.

Amplification is based on the formation of specific hybrids between complementary nucleic acid sequences that serve to initiate nucleic acid reproduction. Amplification can be performed according to various techniques known in the art, such as by polymerase chain reaction (PCR), ligase chain reaction (LCR), strand displacement amplification (SDA) and nucleic acid sequence based amplification (NASBA). These techniques can be performed using commercially available reagents and protocols. Useful techniques in the art encompass real-time PCR, allele-specific PCR, or PCR based single-strand conformational polymorphism (SSCP). Amplification usually requires the use of specific nucleic acid primers, to initiate the reaction. For example, nucleic acid primers useful for amplifying sequences corresponding to an EGFR fusion molecule are able to specifically hybridize with a portion of the gene locus that flanks a target region of the locus. In one embodiment, amplification comprises using forward and reverse PCR primers directed to SEQ ID NOS: 2, 4, 8, 10, 14, or 15. Nucleic acid primers useful for amplifying sequences from an EGFR fusion molecule; the primers specifically hybridize with a portion of an EGFR fusion molecule. In certain subjects, the presence of an EGFR fusion molecule corresponds to a subject with a gene fusion-associated cancer. In one embodiment, amplification can comprise using forward and reverse PCR primers comprising nucleotide sequences of SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, or 89.

Non-limiting amplification methods include, e.g., polymerase chain reaction, PCR (PCR Protocols, A Guide To Methods And Applications, ed. Innis, Academic Press, N.Y., 1990 and PCR Strategies, 1995, ed. Innis, Academic Press, Inc., N.Y.); ligase chain reaction (LCR) (Wu (1989) Genomics 4:560; Landegren (1988) Science 241:1077; Barringer (1990) Gene 89:117); transcription amplification (Kwoh (1989) PNAS 86:1173); and, self-sustained sequence replication (Guatelli (1990) PNAS 87:1874); Q Beta replicase amplification (Smith (1997) J. Clin. Microbiol. 35:1477-1491), automated Q-beta replicase amplification assay (Burg (1996) Mol. Cell. Probes 10:257-271) and other RNA polymerase mediated techniques (e.g., NASBA, Cangene, Mississauga, Ontario; see also Berger (1987) Methods Enzymol. 152:307-316; U.S. Pat. Nos. 4,683,195 and 4,683,202; and Sooknanan (1995) Biotechnology 13:563-564). All the references stated above are incorporated by reference in their entireties.

The invention provides for a nucleic acid primer, wherein the primer can be complementary to and hybridize specifically to a portion of an EGFR fusion molecule, such as a nucleic acid (e.g., DNA or RNA), in certain subjects having a gene fusion-associated cancer. In one embodiment, the gene-fusion associated cancer comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. Primers of the invention can be specific for fusion sequences in a nucleic acid (DNA or RNA) encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. By using such primers, the detection of an amplification product indicates the presence of a fusion of a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. Examples of primers of this invention can be single-stranded nucleic acid molecules of about 5 to 60 nucleotides in length, or about 8 to about 25 nucleotides in length. The sequence can be derived directly from the sequence of an EGFR fusion molecule, e.g. a nucleic acid encoding an EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion. Perfect complementarity is useful to ensure high specificity; however, certain mismatch can be tolerated. For example, a nucleic acid primer or a pair of nucleic acid primers as described above can be used in a method for detecting the presence of a gene fusion-associated cancer in a subject. In one embodiment, primers can be used to detect an EGFR fusion molecule, such as a primer comprising SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, 89; or a combination thereof.

Specific Ligand Binding.

As discussed herein, a nucleic acid encoding an EGFR fusion molecule or expression of an EGFR fusion molecule, can also be detected by screening for alteration(s) in a sequence or expression level of a polypeptide encoded by the same. Different types of ligands can be used, such as specific antibodies. In one embodiment, the sample is contacted with an antibody specific for a polypeptide encoded by an EGFR fusion molecule and the formation of an immune complex is subsequently determined Various methods for detecting an immune complex can be used, such as ELISA, radioimmunoassays (RIA) and immuno-enzymatic assays (IEMA).

For example, an antibody can be a polyclonal antibody, a monoclonal antibody, as well as fragments or derivatives thereof having substantially the same antigen specificity. Fragments include Fab, Fab′2, or CDR regions. Derivatives include single-chain antibodies, humanized antibodies, or poly-functional antibodies. An antibody specific for a polypeptide encoded by an EGFR fusion molecule can be an antibody that selectively binds such a polypeptide. In one embodiment, the antibody is raised against a polypeptide encoded by an EGFR fusion molecule or an epitope-containing fragment thereof. Although non-specific binding towards other antigens can occur, binding to the target polypeptide occurs with a higher affinity and can be reliably discriminated from non-specific binding. In one embodiment, the method can comprise contacting a sample from the subject with an antibody specific for an EGFR fusion molecule, and determining the presence of an immune complex. Optionally, the sample can be contacted to a support coated with antibody specific for an EGFR fusion molecule. In one embodiment, the sample can be contacted simultaneously, or in parallel, or sequentially, with various antibodies specific for different forms of an EGFR fusion molecule, e.g., EGFR-SEPT fusion (such as an EGFR-SEPT14 fusion), an EGFR-CAND fusion (such as an EGFR-CAND1 fusion), or an EGFR-PSPH fusion.

The invention also provides for a diagnostic kit comprising products and reagents for detecting in a sample from a subject the presence of an EGFR fusion molecule. The kit can be useful for determining whether a sample from a subject exhibits reduced expression of an EGFR fusion molecule. For example, the diagnostic kit according to the present invention comprises any primer, any pair of primers, any nucleic acid probe and/or any ligand, or any antibody directed specifically to an EGFR fusion molecule. The diagnostic kit according to the present invention can further comprise reagents and/or protocols for performing a hybridization, amplification, or antigen-antibody immune reaction. In one embodiment, the kit can comprise nucleic acid primers that specifically hybridize to and can prime a polymerase reaction from an EGFR fusion molecule comprising SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, 89, or a combination thereof. In one embodiment, primers can be used to detect an EGFR fusion molecule, such as a primer comprising SEQ ID NOS 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 87, 88, 89; or a combination thereof. In a further embodiment, primers used for the screening of EGFR fusion molecules.

The diagnosis methods can be performed in vitro, ex vivo, or in vivo. These methods utilize a sample from the subject in order to assess the status of an EGFR fusion molecule. The sample can be any biological sample derived from a subject, which contains nucleic acids or polypeptides. Examples of such samples include, but are not limited to, fluids, tissues, cell samples, organs, and tissue biopsies. Non-limiting examples of samples include blood, liver, plasma, serum, saliva, urine, or seminal fluid. The sample can be collected according to conventional techniques and used directly for diagnosis or stored. The sample can be treated prior to performing the method, in order to render or improve availability of nucleic acids or polypeptides for testing. Treatments include, for instance, lysis (e.g., mechanical, physical, or chemical), centrifugation. The nucleic acids and/or polypeptides can be pre-purified or enriched by conventional techniques, and/or reduced in complexity. Nucleic acids and polypeptides can also be treated with enzymes or other chemical or physical treatments to produce fragments thereof. In one embodiment, the sample is contacted with reagents, such as probes, primers, or ligands, in order to assess the presence of an EGFR fusion molecule. Contacting can be performed in any suitable device, such as a plate, tube, well, or glass. In some embodiments, the contacting is performed on a substrate coated with the reagent, such as a nucleic acid array or a specific ligand array. The substrate can be a solid or semi-solid substrate such as any support comprising glass, plastic, nylon, paper, metal, or polymers. The substrate can be of various forms and sizes, such as a slide, a membrane, a bead, a column, or a gel. The contacting can be made under any condition suitable for a complex to be formed between the reagent and the nucleic acids or polypeptides of the sample.

Nucleic Acid Delivery Methods

Delivery of nucleic acids into viable cells can be effected ex vivo, in situ, or in vivo by use of vectors, such as viral vectors (e.g., lentivirus, adenovirus, adeno-associated virus, or a retrovirus), or ex vivo by use of physical DNA transfer methods (e.g., liposomes or chemical treatments). Non-limiting techniques suitable for the transfer of nucleic acid into mammalian cells in vitro include the use of liposomes, electroporation, microinjection, cell fusion, DEAE-dextran, and the calcium phosphate precipitation method (See, for example, Anderson, Nature, 1998) supplement to 392(6679):25( ). Introduction of a nucleic acid or a gene encoding a polypeptide of the invention can also be accomplished with extrachromosomal substrates (transient expression) or artificial chromosomes (stable expression). Cells can also be cultured ex vivo in the presence of therapeutic compositions of the present invention in order to proliferate or to produce a desired effect on or activity in such cells. Treated cells can then be introduced in vivo for therapeutic purposes.

Nucleic acids can be inserted into vectors and used as gene therapy vectors. A number of viruses have been used as gene transfer vectors, including papovaviruses, e.g., SV40 (Madzak et al., (1992) J Gen Virol. 73(Pt 6):1533-6), adenovirus (Berkner (1992) Curr Top Microbiol Immunol. 158:39-66; Berkner (1988) Biotechniques, 6(7):616-29; Gorziglia and Kapikian (1992) J Virol. 66(7):4407-12; Quantin et al., (1992) Proc Natl Acad Sci USA. 89(7):2581-4; Rosenfeld et al., (1992) Cell. 68(1):143-55; Wilkinson et al., (1992) Nucleic Acids Res. 20(9):2233-9; Stratford-Perricaudet et al., (1990) Hum Gene Ther. 1(3):241-56), vaccinia virus (Moss (1992) Curr Opin Biotechnol. 3(5):518-22), adeno-associated virus (Muzyczka, (1992) Curr Top Microbiol Immunol. 158:97-129; Ohi et al., (1990) Gene. 89(2):279-82), herpesviruses including HSV and EBV (Margolskee (1992) Curr Top Microbiol Immunol. 158:67-95; Johnson et al., (1992) Brain Res Mol Brain Res. 12(1-3):95-102; Fink et al., (1992) Hum Gene Ther. 3(1):11-9; Breakefield and Geller (1987) Mol Neurobiol. 1(4):339-71; Freese et al., (1990) Biochem Pharmacol. 40(10):2189-99), and retroviruses of avian (Bandyopadhyay and Temin (1984) Mol Cell Biol. 4(4):749-54; Petropoulos et al., (1992) J Virol. 66(6):3391-7), murine (Miller et al. (1992) Mol Cell Biol. 12(7):3262-72; Miller et al., (1985) J Virol. 55(3):521-6; Sorge et al., (1984) Mol Cell Biol. 4(9):1730-7; Mann and Baltimore (1985) J Virol. 54(2):401-7; Miller et al., (1988) J Virol. 62(11):4337-45), and human origin (Shimada et al., (1991) J Clin Invest. 88(3):1043-7; Helseth et al., (1990) J Virol. 64(12):6314-8; Page et al., (1990) J Virol. 64(11):5270-6; Buchschacher and Panganiban (1992) J Virol. 66(5):2731-9).

Non-limiting examples of in vivo gene transfer techniques include transfection with viral (e.g., retroviral) vectors (see U.S. Pat. No. 5,252,479, which is incorporated by reference in its entirety) and viral coat protein-liposome mediated transfection (Dzau et al., (1993) Trends in Biotechnology 11:205-210), incorporated entirely by reference). For example, naked DNA vaccines are generally known in the art; see Brower, (1998) Nature Biotechnology, 16:1304-1305, which is incorporated by reference in its entirety. Gene therapy vectors can be delivered to a subject by, for example, intravenous injection, local administration (see, e.g., U.S. Pat. No. 5,328,470) or by stereotactic injection (see, e.g., Chen, et al., (1994) Proc. Natl. Acad. Sci. USA 91:3054-3057). The pharmaceutical preparation of the gene therapy vector can include the gene therapy vector in an acceptable diluent, or can comprise a slow release matrix in which the gene delivery vehicle is imbedded. Alternatively, where the complete gene delivery vector can be produced intact from recombinant cells, e.g., retroviral vectors, the pharmaceutical preparation can include one or more cells that produce the gene delivery system.

For reviews of nucleic acid delivery protocols and methods see Anderson et al. (1992) Science 256:808-813; U.S. Pat. Nos. 5,252,479, 5,747,469, 6,017,524, 6,143,290, 6,410,010 6,511,847; and U.S. Application Publication No. 2002/0077313, which are all hereby incorporated by reference in their entireties. For additional reviews, see Friedmann (1989) Science, 244:1275-1281; Verma, Scientific American: 68-84 (1990); Miller (1992) Nature, 357: 455-460; Kikuchi et al. (2008) J Dermatol Sci. 50(2):87-98; Isaka et al. (2007) Expert Opin Drug Deliv. 4(5):561-71; Jager et al. (2007) Curr Gene Ther. 7(4):272-83; Waehler et al. (2007) Nat Rev Genet. 8(8):573-87; Jensen et al. (2007) Ann Med. 39(2):108-15; Herweijer et al. (2007) Gene Ther. 14(2):99-107; Eliyahu et al. (2005) Molecules 10(1):34-64; and Altaras et al. (2005) Adv Biochem Eng Biotechnol. 99:193-260, all of which are hereby incorporated by reference in their entireties.

An EGFR fusion nucleic acid can also be delivered in a controlled release system. For example, the EGFR fusion molecule can be administered using intravenous infusion, an implantable osmotic pump, a transdermal patch, liposomes, or other modes of administration. In one embodiment, a pump can be used (see Sefton (1987) Biomed. Eng. 14:201; Buchwald et al. (1980) Surgery 88:507; Saudek et al. (1989) N. Engl. J. Med. 321:574). In another embodiment, polymeric materials can be used (see Medical Applications of Controlled Release, Langer and Wise (eds.), CRC Pres., Boca Raton, Fla. (1974); Controlled Drug Bioavailability, Drug Product Design and Performance, Smolen and Ball (eds.), Wiley, New York (1984); Ranger and Peppas, (1983) J. Macromol. Sci. Rev. Macromol. Chem. 23:61; see also Levy et al. (1985) Science 228:190; During et al. (1989) Ann. Neurol. 25:351; Howard et al. (1989) J. Neurosurg. 71:105). In yet another embodiment, a controlled release system can be placed in proximity of the therapeutic target thus requiring only a fraction of the systemic dose (see, e.g., Goodson, in Medical Applications of Controlled Release, supra, vol. 2, pp. 115-138 (1984)). Other controlled release systems are discussed in the review by Langer (Science (1990) 249:1527-1533).

Pharmaceutical Compositions and Administration for Therapy

An inhibitor of the invention can be incorporated into pharmaceutical compositions suitable for administration, for example the inhibitor and a pharmaceutically acceptable carrier.

AN EGFR fusion molecule or inhibitor of the invention can be administered to the subject once (e.g., as a single injection or deposition). Alternatively, an EGFR fusion molecule or inhibitor can be administered once or twice daily to a subject in need thereof for a period of from about two to about twenty-eight days, or from about seven to about ten days. AN EGFR fusion molecule or inhibitor can also be administered once or twice daily to a subject for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 times per year, or a combination thereof. Furthermore, an EGFR fusion molecule or inhibitor of the invention can be co-administrated with another therapeutic. Where a dosage regimen comprises multiple administrations, the effective amount of the EGFR fusion molecule or inhibitor administered to the subject can comprise the total amount of gene product administered over the entire dosage regimen.

AN EGFR fusion molecule or inhibitor can be administered to a subject by any means suitable for delivering the EGFR fusion molecule or inhibitor to cells of the subject, such as cancer cells, e.g., glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma. For example, an EGFR fusion molecule or inhibitor can be administered by methods suitable to transfect cells. Transfection methods for eukaryotic cells are well known in the art, and include direct injection of the nucleic acid into the nucleus or pronucleus of a cell; electroporation; liposome transfer or transfer mediated by lipophilic materials; receptor mediated nucleic acid delivery, bioballistic or particle acceleration; calcium phosphate precipitation, and transfection mediated by viral vectors.

The compositions of this invention can be formulated and administered to reduce the symptoms associated with a gene fusion-associated cancer, e.g., glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma, by any means that produces contact of the active ingredient with the agent's site of action in the body of a subject, such as a human or animal (e.g., a dog, cat, or horse). They can be administered by any conventional means available for use in conjunction with pharmaceuticals, either as individual therapeutic active ingredients or in a combination of therapeutic active ingredients. They can be administered alone, but are generally administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.

A therapeutically effective dose of EGFR fusion molecule or inhibitor can depend upon a number of factors known to those or ordinary skill in the art. The dose(s) of the EGFR fusion molecule inhibitor can vary, for example, depending upon the identity, size, and condition of the subject or sample being treated, further depending upon the route by which the composition is to be administered, if applicable, and the effect which the practitioner desires the an EGFR fusion molecule inhibitor to have upon the nucleic acid or polypeptide of the invention. These amounts can be readily determined by a skilled artisan. Any of the therapeutic applications described herein can be applied to any subject in need of such therapy, including, for example, a mammal such as a dog, a cat, a cow, a horse, a rabbit, a monkey, a pig, a sheep, a goat, or a human.

Pharmaceutical compositions for use in accordance with the invention can be formulated in conventional manner using one or more physiologically acceptable carriers or excipients. The therapeutic compositions of the invention can be formulated for a variety of routes of administration, including systemic and topical or localized administration. Techniques and formulations generally can be found in Remmington's Pharmaceutical Sciences, Meade Publishing Co., Easton, Pa. (20^(th) Ed., 2000), the entire disclosure of which is herein incorporated by reference. For systemic administration, an injection is useful, including intramuscular, intravenous, intraperitoneal, and subcutaneous. For injection, the therapeutic compositions of the invention can be formulated in liquid solutions, for example in physiologically compatible buffers such as Hank's solution or Ringer's solution. In addition, the therapeutic compositions can be formulated in solid form and redissolved or suspended immediately prior to use. Lyophilized forms are also included. Pharmaceutical compositions of the present invention are characterized as being at least sterile and pyrogen-free. These pharmaceutical formulations include formulations for human and veterinary use.

According to the invention, a pharmaceutically acceptable carrier can comprise any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration. The use of such media and agents for pharmaceutically active substances is well known in the art. Any conventional media or agent that is compatible with the active compound can be used. Supplementary active compounds can also be incorporated into the compositions.

A pharmaceutical composition containing EGFR fusion molecule inhibitor can be administered in conjunction with a pharmaceutically acceptable carrier, for any of the therapeutic effects discussed herein. Such pharmaceutical compositions can comprise, for example antibodies directed to an EGFR fusion molecule, or a variant thereof, or antagonists of an EGFR fusion molecule. The compositions can be administered alone or in combination with at least one other agent, such as a stabilizing compound, which can be administered in any sterile, biocompatible pharmaceutical carrier including, but not limited to, saline, buffered saline, dextrose, and water. The compositions can be administered to a patient alone, or in combination with other agents, drugs or hormones.

Sterile injectable solutions can be prepared by incorporating the EGFR fusion molecule inhibitor (e.g., a polypeptide or antibody) in the required amount in an appropriate solvent with one or a combination of ingredients enumerated herein, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated herein. In the case of sterile powders for the preparation of sterile injectable solutions, examples of useful preparation methods are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

In some embodiments, the EGFR fusion molecule inhibitor can be applied via transdermal delivery systems, which slowly releases the active compound for percutaneous absorption. Permeation enhancers can be used to facilitate transdermal penetration of the active factors in the conditioned media. Transdermal patches are described in for example, U.S. Pat. No. 5,407,713; U.S. Pat. No. 5,352,456; U.S. Pat. No. 5,332,213; U.S. Pat. No. 5,336,168; U.S. Pat. No. 5,290,561; U.S. Pat. No. 5,254,346; U.S. Pat. No. 5,164,189; U.S. Pat. No. 5,163,899; U.S. Pat. No. 5,088,977; U.S. Pat. No. 5,087,240; U.S. Pat. No. 5,008,110; and U.S. Pat. No. 4,921,475.

“Subcutaneous” administration can refer to administration just beneath the skin (i.e., beneath the dermis). Generally, the subcutaneous tissue is a layer of fat and connective tissue that houses larger blood vessels and nerves. The size of this layer varies throughout the body and from person to person. The interface between the subcutaneous and muscle layers can be encompassed by subcutaneous administration. This mode of administration can be feasible where the subcutaneous layer is sufficiently thin so that the factors present in the compositions can migrate or diffuse from the locus of administration. Thus, where intradermal administration is utilized, the bolus of composition administered is localized proximate to the subcutaneous layer.

Administration of the cell aggregates (such as DP or DS aggregates) is not restricted to a single route, but can encompass administration by multiple routes. For instance, exemplary administrations by multiple routes include, among others, a combination of intradermal and intramuscular administration, or intradermal and subcutaneous administration. Multiple administrations can be sequential or concurrent. Other modes of application by multiple routes will be apparent to the skilled artisan.

In other embodiments, this implantation method will be a one-time treatment for some subjects. In further embodiments of the invention, multiple cell therapy implantations will be required. In some embodiments, the cells used for implantation will generally be subject-specific genetically engineered cells. In another embodiment, cells obtained from a different species or another individual of the same species can be used. Thus, using such cells can require administering an immunosuppressant to prevent rejection of the implanted cells. Such methods have also been described in U.S. Pat. No. 7,419,661 and PCT application publication WO 2001/32840, and are hereby incorporated by reference.

A pharmaceutical composition of the invention is formulated to be compatible with its intended route of administration. Examples of routes of administration include parenteral, e.g., intravenous, intradermal, subcutaneous, oral (e.g., inhalation or ingestion), transdermal (topical), transmucosal, and rectal administration. Solutions or suspensions used for parenteral, intradermal, or subcutaneous application can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfate; chelating agents such as ethylenediaminetetraacetic acid; buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose. pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. The parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.

Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, or phosphate buffered saline (PBS). In all cases, the composition must be sterile and should be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, a pharmaceutically acceptable polyol like glycerol, propylene glycol, liquid polyetheylene glycol, and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many cases, it can be useful to include isotonic agents, for example, sugars, polyalcohols such as mannitol, sorbitol, sodium chloride in the composition. Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate and gelatin.

Sterile injectable solutions can be prepared by incorporating the inhibitor (e.g., a polypeptide or antibody or small molecule) of the invention in the required amount in an appropriate solvent with one or a combination of ingredients enumerated herein, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated herein. In the case of sterile powders for the preparation of sterile injectable solutions, examples of useful preparation methods are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

Oral compositions generally include an inert diluent or an edible carrier. They can be enclosed in gelatin capsules or compressed into tablets. For the purpose of oral therapeutic administration, the active compound can be incorporated with excipients and used in the form of tablets, troches, or capsules. Oral compositions can also be prepared using a fluid carrier and subsequently swallowed.

Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition. The tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate or sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.

Systemic administration can also be by transmucosal or transdermal means. For transmucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives. Transmucosal administration can be accomplished through the use of nasal sprays or suppositories. For transdermal administration, the active compounds are formulated into ointments, salves, gels, or creams as generally known in the art.

In some embodiments, the effective amount of the administered EGFR fusion molecule inhibitor is at least about 0.0001 μg/kg body weight, at least about 0.00025 μg/kg body weight, at least about 0.0005 μg/kg body weight, at least about 0.00075 μg/kg body weight, at least about 0.001 μg/kg body weight, at least about 0.0025 μg/kg body weight, at least about 0.005 μg/kg body weight, at least about 0.0075 μg/kg body weight, at least about 0.01 μg/kg body weight, at least about 0.025 μg/kg body weight, at least about 0.05 μg/kg body weight, at least about 0.075 μg/kg body weight, at least about 0.1 μg/kg body weight, at least about 0.25 μg/kg body weight, at least about 0.5 μg/kg body weight, at least about 0.75 μg/kg body weight, at least about 1 μg/kg body weight, at least about 5 μg/kg body weight, at least about 10 μg/kg body weight, at least about 25 μg/kg body weight, at least about 50 μg/kg body weight, at least about 75 μg/kg body weight, at least about 100 μg/kg body weight, at least about 150 μg/kg body weight, at least about 200 μg/kg body weight, at least about 250 μg/kg body weight, at least about 300 μg/kg body weight, at least about 350 μg/kg body weight, at least about 400 μg/kg body weight, at least about 450 μg/kg body weight, at least about 500 μg/kg body weight, at least about 550 μg/kg body weight, at least about 600 μg/kg body weight, at least about 650 μg/kg body weight, at least about 700 μg/kg body weight, at least about 750 μg/kg body weight, at least about 800 μg/kg body weight, at least about 850 μg/kg body weight, at least about 900 μg/kg body weight, at least about 950 μg/kg body weight, at least about 1000 μg/kg body weight, at least about 2000 μg/kg body weight, at least about 3000 μg/kg body weight, at least about 4000 μg/kg body weight, at least about 5000 μg/kg body weight, at least about 6000 μg/kg body weight, at least about 7000 μg/kg body weight, at least about 8000 μg/kg body weight, at least about 9500 μg/kg body weight, or at least about 10,000 μg/kg body weight.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Exemplary methods and materials are described below, although methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present invention.

All publications and other references mentioned herein are incorporated by reference in their entirety, as if each individual publication or reference were specifically and individually indicated to be incorporated by reference. Publications and references cited herein are not admitted to be prior art.

EXAMPLES

Examples are provided below to facilitate a more complete understanding of the invention. The following examples illustrate the exemplary modes of making and practicing the invention. However, the scope of the invention is not limited to specific embodiments disclosed in these Examples, which are for purposes of illustration only, since alternative methods can be utilized to obtain similar results.

Example 1 The Integrated Landscape of Driver Genomic Alterations in Glioblastoma

To address the challenge of driver mutations in glioblastoma (GBM) and uncover new driver genes in human GBM, a computational platform was developed that integrates the analysis of copy number variations and somatic mutations from a whole-exome dataset. The full spectrum of in-frame gene fusions was unveiled from a large transcriptome dataset of glioblastoma. The analyses revealed focal copy number variations and mutations in all the genes previously implicated in glioblastoma pathogenesis. Recurrent copy number variations and somatic mutations were detected in 18 genes not yet implicated in glioblastoma. For each of the new genes, the occurrence of focal and recurrent copy number changes in addition to somatic mutations underscores the relevance for glioblastoma pathogenesis. Without being bound by theory, mutations in LZTR-1, a Keltch-BTB-BACK-BTB-BACK adaptor of Cul3-containing E3 ligase complexes impacted ubiquitination of LZTR-1 substrates. Loss-of-function mutations of CTNND2 (coding for δ-catenin) targeted a neural-specific gene and were associated with the transformation of glioma cells along the mesenchymal lineage, a hallmark of aggressive glioblastoma. Reconstitution of δ-catenin in mesenchymal glioma cells reprogrammed them towards a neuronal cell fate. Recurrent translocations were also identified that fuse in-frame the coding sequence of EGFR to several partners in 7.6% of tumors, with EGFR-Septin-14 scoring as the most frequent functional gene fusion in human glioblastoma. EGFR fusions enhance proliferation and motility of glioma cells and confer sensitivity to EGFR inhibition in glioblastoma xenografts. These results provide important insights into the pathogenesis of glioblastoma and highlight new targets for therapeutic intervention.

Glioblastoma (GBM) is the most common primary intrinsic malignant brain tumor affecting ˜10,000 new patients each year with a median survival rate of only 12-15 months^(1,2). Identifying and understanding the functional significance of the genetic alterations that drive initiation and progression of GBM is crucial to develop more effective therapies. Previous efforts in GBM genome characterization included array-based profiling of copy number changes, methylation and gene expression and targeted sequencing of candidate genes³⁻⁶. These studies identified somatic changes in well-known GBM genes (EGFR, PTEN, IDH1, TP53, NF1, etc.) and nominated putative cancer genes with somatic mutations, but the functional consequences of most alterations is unknown. The lack of strict correlation between somatic alterations and functionality in GBM is manifested by regions of large copy number variations (CNVs), in which the relevant gene(s) are masked within genomic domains encompassing many other genes. Furthermore, although the potential of next-generation sequencing of the whole coding exome is widely recognized for the nomination of new cancer genes, the elevated somatic mutation rate of GBM is a significant challenge for statistical approaches aimed to distinguish genes harboring driver from those with passenger mutations. A statistical approach was used to nominate driver genes in GBM from the integration of whole-exome sequencing data calling for somatic mutations with a CNVs analysis that prioritizes focality and magnitude of the genetic alterations.

Chromosomal rearrangements resulting in recurrent and oncogenic gene fusions are hallmarks of hematological malignancies and recently they have also been uncovered in solid tumors (breast, prostate, lung and colorectal carcinoma)^(7,8). Recently, a small subset of GBM harbor FGFR-TACC gene fusions were provided indicating that the patients with FGFR-TACC-positive tumors would benefit from targeted EGFR kinase inhibition⁹. It remains unknown whether gene fusions involving other RTK-coding genes exist in GBM to create different oncogene addicting states. A large RNA-sequencing dataset of primary GBM and glioma stem cells (GSCs) was analyzed and the global landscape of in-frame gene fusions in human GBM was reported.

Nomination of Candidate GBM Genes

Focal CNVs and point mutations provide exquisite information on candidate driver genes by pinpointing their exact location. Without being bound by theory, the integration of somatic point mutations and focal CNV information in a single framework will nominate candidate genes implicated in GBM. MutComFocal is an algorithm designed for this purpose, in which driver genes are ranked by an integrated recurrence, focality and mutation score (see Methods). Overall, this strategy was applied to a cohort of 139 GBM and matched normal DNA analyzed by whole exome sequencing to identify somatic mutations and 469 GBM were analyzed by the Affymetrix SNP6.0 platform to identify CNVs.

The whole-exome analysis identified a mean of 43 protein-changing somatic mutations per tumor sample. The distribution of substitutions shows a higher rate of transitions vs tranversions (67%), with a strong preference for C→T and G→A (55%) (FIG. 6). As seen in other tumor types¹⁰, 19.2% of the mutations occurred in a CpG dinucleotide context (FIG. 7). Among somatic small nucleotide variants, the most frequently mutated genes have well-established roles in cancer, including GBM (TP53, EGFR, PTEN, and IDH1). In addition to known cancer genes, whole-exome sequencing identified several potentially new candidate driver genes mutated in ˜5% of tumor samples. To uncover the most likely driver genes of GBM initiation and/or progression, the mutation results were integrated with common focal genomic alterations, detected using an algorithm applied to high-density SNP arrays to generate MutComFocal scores. This analysis stratified somatically mutated genes into three groups: recurrently mutated genes without significant copy number alterations (Mut), mutated genes in regions of focal and recurrent amplifications (Amp-Mut) and mutated genes in regions of focal and recurrent deletions (Del-Mut). Employing this framework, a list of 67 genes was generated that score at the top of each of the three categories and that included nearly all the genes previously implicated in GBM. These genes, which are labeled in green in FIG. 1 include IDH1 (Mut, FIG. 1a ), PIK3C2B, MDM4, MYCN, PIK3CA, PDGFRA, KIT, EGFR, and BRAF (Amp-Mut, FIG. 1b ) and PIK3R1, PTEN, RB1, TP53, NF1 and A TRX (Del-Mut, FIG. 1c ). Interestingly, the analysis also selected 52 new candidate driver genes previously unreported in GBM. Based upon their role in development and homeostasis of the CNS and their potential function in oncogenesis and tumor progression, 24 genes were selected for re-sequencing in an independent dataset of 35 GBM and matched normal controls. Eighteen genes were found somatically mutated by Sanger sequencing in the independent panel and are labeled in red in FIG. 1. Each of the validated new GBM genes is targeted by somatic mutations and CNVs in a cumulative fraction comprised between 2.9% and 45.7% of GBM (FIG. 9).

Among the commonly mutated and focally deleted genes that exhibited top MutComFocal scores and were validated in the independent GBM dataset, BCOR, LRP family members, HERC2, LZTR-1 and CTNND2. BCOR, a chromosome X-linked gene, encodes for a component of the nuclear co-repressor complex that is essential for normal development of the neuroectoderm and stem cell functions¹¹⁻¹³. BCOR mutations have recently been described in retinoblastoma and medulloblastoma, thus indicating that loss-of-function mutations in BCOR are common genetic events in neuroectodermal tumors^(14,15). LRP1B is a member of the LDL receptor family and is among the most frequently mutated genes in human cancer (FIG. 1c )¹⁶. Interestingly, two other LDL receptor family members (LRP2 and LRP1) are mutated in 4.4% and 2.9% of tumors, respectively (FIG. 1a ). The LRP proteins are highly expressed in the neuroepithelium and are essential for morphogenesis of the forebrain in mouse and humans^(17,18). The tumor suppressor function of LRP proteins in GBM may be linked to their ability to promote chemosensitivity and control signaling through the Sonic hedgehog pathway, which is responsible for maintenance of cancer initiating cells in GBM¹⁹⁻²¹. The gene coding for the Hect ubiquitin ligase Herc2 is localized on chromosome 15q13 and is deleted and mutated in 15.1% and 2.2% of GBM cases, respectively. This gene has been implicated in severe neurodevelopmental syndromes. Moreover, protein substrates of Herc2 are crucial factors in genome stability and DNA damage-repair, two cell functions frequently disrupted in cancer^(22,23).

Loss-of-Function Genetic Alterations Target the LZTR-1 and CTNND2 Genes in GBM

A gene that received one of the highest Del-Mut score by MutComFocal is LZTR-1 (FIG. 1c ). The LZTR-1 coding region had non-synonymous mutations in 4.4% and the LZTR-1 locus (human chromosome 22q11) was deleted in 22.4% of GBM. LZTR-1, which is normally expressed in the human brain, codes for a protein with a characteristic Kelch-BTB-BACK-BTB-BACK domain architecture (FIGS. 8, 9). The LZTR-1 gene is highly conserved in the metazoans and was initially proposed to function as a transcriptional regulator, but follow-up studies have excluded a transcriptional role for this protein²⁴. Most proteins with BTB-BACK domains are substrate adaptors in Cullin3 (Cul3) ubiquitin ligase complexes, in which the BTB-BACK region binds to the N-terminal domain of Cul3, while a ligand binding domain, often a Kelch 6-bladed β-propeller motif, binds to substrates targeted for ubiquitination²⁵. To ask whether LZTR-1 directly binds Cul3, co-immunoprecipitation experiments were performed. FIG. 2a shows that Cul3 immunoprecipitates contain LZTR-1, thus indicating that LZTR-1 is an adaptor in Cul3 ubiquitin ligase complexes.

To address the potential function of LZTR-1 mutants, a homology model of LZTR-1 was built based in part on the crystal structures of the MATH-BTB-BACK protein SPOP²⁶, the BTB-BACK-Kelch proteins KLHL3 and KLHL11²⁷, and the Kelch domain of Keap1²⁸ (FIG. 2b ). Without being bound by theory, the second BTB-BACK region of LZTR-1 binds Cul3 because of the presence of φ-X-E motif in this BTB domain, followed by a 3-Box/BACK region (FIG. 9)²⁶. However, the preceding BTB-BACK region also participates in Cul3 binding. Four of the six LZTR-1 mutations identified in GBM are located within the Kelch domain and target highly conserved amino acids (FIG. 2b, c , FIG. 8). Interestingly, the concentration of LZTR-1 mutations in the Kelch domain reflects a similar pattern of mutations in the Kelch-coding region of the KLHL3 gene, recently identified in families with hypertension and electrolytic abnormalities^(29,30). The R198G and G248R mutations localize to the b-c loop of the Kelch domain, in a region predicted to provide the substrate-binding surface of the domain²⁸. The W105R mutation targets a highly conserved anchor residue in the Kelch repeats and the T288I mutation disrupts a buried residue that is conserved in LZTR-1 (FIG. 2b , FIG. 8). Both of these mutations are expected to perturb the folding of the Kelch domain. The remaining two mutations, located in the BTB-BACK domains are predicted to affect the interaction with Cul3 either by removing the entire BTB-BACK-BTB-BACK region (W437STOP) or by disrupting the folding of the last helical hairpin in the BTB-BACK domain (R810W, FIG. 2b ). The pattern of mutations of LZTR-1 in GBM indicates that they impair binding either to specific substrates or to Cul3.

Among the top ranking genes in MutComFocal, CTNND2 is the gene expressed at the highest levels in the normal brain. CTNND2 codes for -catenin, a member of the p120 subfamily of catenins that is expressed almost exclusively in the nervous system where it is crucial for neurite elongation, dendritic morphogenesis and synaptic plasticity³¹⁻³³. Germ-line hemizygous loss of CTNND2 severely impairs cognitive function and underlies some forms of mental retardation^(34,35). CTNND2 shows a pronounced clustering of mutations in GBM. The observed spectrum of mutations includes four mutations located in the armadillo-coding domain and one in the region coding for the N-terminal coiled-coil domain (FIG. 10a ). These regions are the two most relevant functional domains of δ-catenin and each of the mutations targets highly conserved residues with probably (K629Q, A776T, S881L, D999E) and possibly (A71T) damaging consequences³⁶. Together with focal genomic losses of CTNND2 (FIG. 10b ), the mutation pattern indicates that CTNND2 is a tumor suppressor gene in GBM.

It was asked whether the expression of CTNND2 is down-regulated during oncogenic transformation in the CNS Immunostaining experiments showed that δ-catenin is strongly expressed in the normal human and mouse brain with the highest expression in neurons (FIG. 3a , FIG. 10c ). Conversely, the immunostaining analysis of 69 GBM revealed negligible or absent expression of δ-catenin in 21 cases (FIG. 3b ). Oncogenic transformation in the CNS frequently results in loss of the default proneural cell fate in favor of an aberrant mesenchymal phenotype, which is associated with a very aggressive clinical outcome³⁷. The analysis of gene expression profiles of 498 GBM from the ATLAS-TCGA collection showed that low expression of CTNND2 is strongly enriched in tumors identified by a mesenchymal gene expression signature (T-test p-value=2.4 10⁻¹², FIG. 10d ). Tumors with low CTNND2 expression were also characterized by poor clinical outcome and, among them tumors with copy number losses of the CTNND2 gene displayed the worst prognosis (FIG. 3c, d ). Mesenchymal transformation of GBM, which is detected in the vast majority of established glioma cell lines, is associated with an apparently irreversible loss of the proneural cell fate and neuronal markers³⁷. Expression of δ-catenin in the U87 human glioma cell line reduced cell proliferation (FIG. 3e ), decreased the expression of mesenchymal markers (FIG. 3f ) and induced neuronal differentiation as shown by elongation of β3-tubulin-positive neurites and development of branched dendritic processes that stained positive for the post-synaptic marker PSD95 (FIG. 3g ). Accordingly, δ-catenin decreased expression of cyclin A, a S-phase cyclin and up-regulated the Cdk inhibitor p27^(Kip1) and the neuronal-specific gene N-cadherin (FIG. 3h ). Thus, restoring the normal expression of δ-catenin reprograms mesenchymal glioma cells towards the proneural lineage.

Recurrent EGFR Fusions in GBM

To identify gene fusions in GBM, RNA-seq data was analyzed from a total of 185 GBM samples (161 primary GBM plus 24 short-term cultures of glioma stem-like cells (GSCs) freshly isolated from patients carrying primary GBM). The analysis of the RNA-seq dataset led to the discovery of 92 candidate rearrangements that give rise to in-frame fusion transcripts (Table 7). Beside the previously reported FGFR3-TACC3 fusions events, the most frequent recurrent in-frame fusions involved EGFR in 7.6% of samples (14/185, 3.8%-11.3% CI). Nine of the 14 EGFR fusions included the recurrent partners SEPT14 (6/185, 3.2%) and PSPH (3/185, 1.6%) as the 3′ gene segment in the fusion. Two in-frame highly expressed fusions were also found involving the neurotrophic tyrosine kinase receptor 1 gene (NTRK1) as 3′ gene with two different 5′ partners (NFASC-NTRK1 and BCAN-NTRK1). Fusions with a similar structure involving NTRK1 are commonly found in papillary thyroid carcinomas³⁸. Using EXomeFuse, an algorithm for the reconstruction of genomic fusions from whole-exome data, EGFR-SEPT14 and NRTK1 fusions are the result of recurrent chromosomal translocations and reconstructed the corresponding genomic breakpoints (Table 8).

By sequencing the PCR products spanning the fusion breakpoint, each of the three types of recurrent in-frame fusion predictions (EGFR-SEPT14, EGFR-PSPH and NRTK1 fusions, FIG. 4, FIG. 11, and FIG. 12) were validated. In FIG. 4a, b the prediction and cDNA sequence validation are shown, respectively, for one of the tumors harboring an EGFR-SEPT14 fusion (TCGA-27-1837). The amplified cDNA contained an open reading frame for a protein of 1,041 amino acids resulting from the fusion of an EGFR amino-terminal portion of residues 1-982 with a SEPT14 carboxy-terminal portion of residues 373-432 (FIG. 4c ). Thus, the structure of the EGFR-Septin14 fusion proteins involves EGFR at the N-terminus, providing a receptor tyrosine kinase domain fused to a coiled-coil domain from Septin14. Exon-specific gene expression analysis from the RNA-seq coverage in TCGA-27-1837 demonstrated that the EGFR and SEPT14 exons implicated in the fusion are highly overexpressed compared with the mRNA sequences not included in the fusion event (FIG. 13). Using PCR, the genomic breakpoint coordinates were mapped to chromosome 7 (#55,268,937 for EGFR and #55,870,909 for SEPT14, genome build GRCh37/hg19) falling within EGFR exon 25 and SEPT14 intron 9, which gives rise to a transcript in which the 5′ EGFR exon 24 is spliced to the 3′ SEPT14 exon 10 (FIG. 4d ). Interestingly, the fused EGFR-PSPH cDNA and predicted fusion protein in the GBM sample TCGA-06-5408 involves the same EGFR N-terminal region implicated in the EGFR-SEPT14 with PSPH providing a carboxy-terminal portion of 35 amino acids (FIG. 11). An example of a fusion in which the EGFR-TK region is the 3′ partner is the CAND1-EGFR fusion in GSC-3316 (FIG. 14). Thus, either in the more frequent fusions in which EGFR is the 5′ partner or in those with EGFR as the 3′ gene, the region of the EGFR mRNA coding for the TK domain is invariably retained in each of the fusion transcripts (Table 7). RT-PCR and genomic PCR followed by Sanger sequencing from GBM TCGA-06-5411 were also used to successfully validate successfully the NFASC-NTRK1 fusions in which the predicted fusion protein includes the TK domain of the high-affinity NGF receptor (TrkA) fused downstream to the immunoglobulin-like region of the cell adhesion and ankyrin-binding region of neurofascin (FIG. 12).

To confirm that GBM harbor recurrent EGFR fusions and determine the frequency in an independent dataset, cDNA was screened from a panel of 248 GBMs and discovered 10 additional cases harboring EGFR-SEPT14 fusions (4%). Conversely, NFASC-NTRK1 fusions were not detected in this dataset. The frequency of EGFR-PSPH fusions was 2.2% (3/135).

The discovery of recurrent EGFR fusions in GBM is of particular interest. EGFR is activated in a significant fraction of primary GBM (˜25%) by an in-frame deletion of exons 2-7 (EGFRvIII)³⁹. To establish the functional relevance of EGFR fusions, it was determined whether the most frequent EGFR fusion in GBM (EGFR-SEPT14) provides an alternative mechanism of EGFR activation and confers sensitivity to EGFR inhibition. The EGFR-SEPT14 cDNA was cloned and prepared lentiviruses expressing EGFR-SEPT14, EGFRvIII or EGFR wild type. Transduction of the SNB19 glioma cell line (which lacks genomic alteration of EGFR) with the recombinant lentiviruses showed that cells expressing EGFR-SEPT14 or EGFRvIII proliferated at a rate that was 2-fold higher than control cells or cells expressing wild type EGFR (FIG. 5a ). Furthermore, EGFR-SEPT14 and EGFRvIII markedly enhanced the ability of SNB19 cells to migrate in a wound assay (FIG. 5b, c ). Finally it was investigated whether EGFR-SEPT14 fusions confer sensitivity to EGFR-TK activity in vivo. The analysis of a collection of 30 GBM xenografts directly established in the mouse from human GBM identified one xenograft model (D08-0537 MG) harboring the EGFR-SEPT14 fusion. The D08-0537 MG had been established from a heavily pretreated GBM. Treatment of D08-0537 MG tumors with two EGFR inhibitors showed that each of the two drugs significantly delayed the rate of tumor growth (FIG. 5d ). Interestingly, lapatinib, an irreversible EGFR inhibitor recently proposed to target EGFR alterations in GBM⁴⁰, displayed the strongest anti-tumor effects (FIG. 5d, e ). Conversely, EGFR inhibitors were ineffective against the GBM xenograft D08-0714 MG, which lacks genomic alterations of the EGFR gene (FIG. 5d, e ). Taken together, these data determine that the EGFR-SEPT14 fusion confers a proliferative and migratory phenotype to glioma cells and imparts sensitivity to EGFR inhibition to human glioma harboring the fusion gene.

Discussion

A computational pipeline is described for the nomination of somatic cancer genes. This approach computes frequency, magnitude and focality of CNVs at any loci in the human genome with the somatic mutation rate for the genes residing at that genomic location. Thus, two of the genetic hallmarks of driver cancer genes (focality of copy number aberrations and point mutations) are integrated into a single score. The approach identifies marks of positive somatic selection in large unbiased cancer genome studies by efficiently removing the large burden of passenger mutations that characterize most human tumors and will be applicable to the dissection of the genomic landscape of other cancer types.

Besides recognizing nearly all the known genes reported to have functional relevance in GBM, our study discovered and validated somatic mutations in 18 new genes, which also harbor focal and recurrent CNVs in a significant fraction of GBM. For some of these genes, their importance extends beyond GBM, as underscored by cross-tumor relevance (e.g. BCOR), and protein family recurrence (e.g. LRP family members). For example, mutations of LZTR-1 have been reported in other tumors. In particular, mutations of the highly conserved residues in the Keltch domain (W105, G248, T288) and in the second BTB-BACK domain (R810) reported here are recurrent events in other tumor types⁴¹. Thus, understanding the nature of the substrates of LZTR-1-Cul3 ubiquitin ligase activity will provide important insights into the pathogenesis of multiple cancer types.

The identification of genetic and epigenetic loss-of-function alterations of the CTNND2 gene clustered in mesenchymal GBM provides a clue to the genetic events driving this aggressive GBM subtype. The important functions of δ-catenin for such crucial neuronal morphogenesis activities as the coordinated control of axonal and dendritic arborization indicates that full-blown mesenchymal transformation in the brain requires loss of the master regulators constraining cell determination in the CNS along the default neuronal lineage. The ability of δ-catenin to reprogram glioma cells that express mesenchymal genes towards a neuronal fate unravels an unexpected plasticity of mesenchymal GBM that might be exploited therapeutically.

In this study, the landscape of gene fusions is reported from a large dataset of GBM analyzed by RNA-Sequencing. In-frame gene fusions retaining the RTK-coding domain of EGFR emerged as the most frequent gene fusion events in GBM. In this tumor, EGFR is frequently targeted by focal amplications and our finding underscores the strong recombinogenic probability of focally amplified genes, as recently reported for the myc locus in medulloblastoma⁴². Resembling intragenic rearrangements that generate the EGFRvIII allele, EGFR-SEPT14 fusions enhance the proliferative and migratory capacity of glioma cells. They also confer sensitivity to EGFR inhibition to human GBM grown as mouse xenografts. These findings highlight the relevance of gene fusions implicating RTK-coding genes in the pathogenesis of GBM⁹. They also provide a strong rationale for the inclusion of GBM patients harboring EGFR fusions in clinical trials based on EGFR inhibitors.

Methods

139 paired tumor-normal samples from TCGA were analyzed with the SAVI pipeline⁴³. The SAVI algorithm estimates frequencies of variant alleles in sample as well as the difference in allele frequency between paired samples. The algorithm establishes posterior high credibility intervals for those frequencies and differences of frequencies, which can be used for genotyping the samples on the one hand, and detecting somatic mutations in the case of tumor/normal pairs of samples on the other. The algorithm allows for random sequencing errors and uses the Phred scores of the sequenced alleles as an estimate of their reliability. To integrate point mutation and 469 GBM CNV data (Affymetrix SNP6.0), MutComFocal (see below) was used. The MutComFocal algorithm assigns a driver score to each gene through three different strategies that give priority to lesions, samples, and genes in which there is less uncertainty regarding potential tumorigenic drivers. First, the focality component of the score is inversely proportional to the size of the genomic lesion to which a gene belongs and thus prioritizes more focal genomic lesions. Second, the recurrence component of the MutComFocal score is inversely proportional to the total number of genes altered in a sample, which prioritizes samples with a smaller number of altered genes. Finally, the mutation component of the score is inversely proportional to the total number of genes mutated in a sample, which achieves the two-fold goal of prioritizing mutated genes on one hand, and samples with a smaller number of mutations on the other.

161 RNA-Seq GBM tumor samples were also analyzed from TCGA plus 24 generated from our own dataset of GSCs. Nine of these samples previously reported in other studies were kept in the list to evaluate recurrence⁹. The samples were analyzed by means of the ChimeraScan algorithm in order to detect a list of gene fusion candidates⁴⁴. Using the Pegasus annotation pipeline (http://sourceforge.net/projects/pegasus-fus/), the fusion transcript was reconstructed, the reading frame was annotated and protein domains were detected that are either conserved or lost in the new chimeric event. The genomic breakpoint of recurrent gene fusion RNA transcripts was also probed for using whole-exome sequencing data (EXome-Fuse algorithm)⁹. The Kaplan-Meier survival analysis for CTNND2 CNV and CTNND2 expression were obtained using the REMBRANDT glioma dataset.

SAVI (Statistical Algorithm for Variant Frequency Identification):

The frequency of alleles in a sample was estimated by the SAVI pipeline, which constructs an empirical Bayesian prior for those frequencies, using data from the whole sample, and obtains a posterior distribution and high credibility intervals for each allele^(S1). The prior and posterior are distributed over a discrete set of frequencies with a precision of 1% and are connected by a modified binomial likelihood, which allows for some error rate. More precisely, a prior distribution p(f) of the frequency f and a prior for the error e uniform on the interval [0, E] was assumed for a fixed 0≦E≦1. The sequencing data at a particular allele is a random experiment producing a string of m (the total depth at the allele) bits with n “1” s (the variant depth at the allele). Assuming a binomial likelihood of the data and allowing for bits being misread due to random errors, the posterior probability P(f) of the frequency f is

${P(f)} = {{\frac{p(f)}{C} \cdot \frac{1}{b - 1}}{\int_{f}^{f + E - {2{Ef}}}{{x^{n}\left( {1 - x} \right)}^{m - n}{x}}}}$

where C is a normalization constant. For a particular allele, the value of E is determined by the quality of the nucleotides sequenced at that position as specified by their Phred scores. The SAVI pipeline takes as input the reads produced by the sequencing technology, filters out low quality reads and maps the rest onto a human reference genome. After mapping, a Bayesian prior for the distribution of allele frequencies for each sample is constructed by an iterative posterior update procedure, starting with a uniform prior. To genotype the sample, the posterior high credibility intervals were used for the frequency of the alleles at each genomic location. Alternatively, combining the Bayesian priors from different samples, posterior high credibility intervals were obtained for the difference between the samples of the frequencies of each allele. Finally, the statistically significant differences between the tumor and normal samples are reported as somatic variants. To estimate the positive prediction value of SAVI in the TCGA GBM samples, 41 mutations were selected for independent validation by Sanger sequencing. 39 of the 41 mutations were confirmed using Sanger sequencing, resulting in 0.95 (95% CI 0.83-0.99) validation rate.

Candidate genes were ranked by the number of somatic non-synonymous mutations. A robust fit of the ratio of non-synonymous to synonymous ratio was generated with a bisquare weighting function. Excess of non-synonymous alterations was estimated using a Poisson distribution with mean equal to the product of the ratio from the robust fit and the number of synonymous mutations. Genes in highly polymorphic genomic regions were filtered out based on an independent cohort of normal samples. The list of these regions includes families of genes known to generate false positives in somatic predictions (e.g. HLA, KRT and OR).

MutComFocal.

Key cancer genes are often found amplified or deleted in chromosomal regions containing many other genes. Point mutations and gene fusions, on the other hand, provide more specific information about which genes may be implicated in the oncogenic process. MutComFocal, a Bayesian approach aiming to identify driver genes by integrating CNV and point mutation data was developed.

For a particular sample, let (c₁, N₁), . . . , (c_(k), N_(k)) describe the amplification lesions in that sample so that N_(i) is the number of genes in the i-th lesion and c_(i) is its copy number change from normal. For a gene belonging to the i-th lesion the amplification recurrence sample score is defined as c_(i)/(Σ_(j)c_(j)·N_(j)) and its amplification focality sample score is defined as (c_(i)/Σ_(j) c_(j))·(1/N_(i)). To obtain the amplification recurrence and focality scores for a particular gene, the corresponding sample scores were summed over all samples and normalize the result so that each score sums to 1. The deletion and recurrence scores are defined in a similar manner. The mutation score is analogous to a recurrence score in which it was assumed that mutated genes belong to lesions with only one gene.

The amplification/mutation score is defined as the product of the two amplification scores and the mutation score while deletion/mutation score is defined as the product of the two deletion scores and the mutation score. The amplification/mutation and deletion/mutation scores are normalized to 1 and for each score, genes are divided into tiers iteratively, so that the top 2^(H) remaining genes are included in the next tier, where H is the entropy of the scores of the remaining genes normalized to 1. Based on their tier across the different types of scores, genes are assigned to being either deleted/mutated or amplified/mutated and genes in the top tiers are grouped into contiguous regions. The top genes in each region are considered manually and selected for further functional validation.

The recurrence and focality scores can be interpreted as the posterior probabilities that a gene is driving the selection of the disease, under two different priors for this: one global and one local in nature. The recurrence score is higher if a gene participates in many samples that do not have too many altered genes, while the focality score is higher if the gene participates in many focal lesions. Besides lending strong support to the inference of a gene as a potential driver, the directionality of the copy number alteration (amplification or deletion) informs us of the likely behavior of the candidate gene as an oncogene or tumor suppressor, respectively.

The genes displayed in FIG. 1 are selected based on the MutComFocal ranking (top 250 genes), the size of minimal region (less than 10 genes) and frequency of mutations (more than 2% for deletion/mutations and at least 1% in amplification/mutations).

RNA-Seq Bioinformatics Analysis.

161 RNA-Seq GBM tumor samples were analyzed from The Cancer Genome Atlas (TCGA), a public repository containing large-scale genome-sequencing of different cancers, plus 24 patients-derived GSCs. Nine of the GSCs samples reported in previous studies were kept in the list to evaluate recurrence^(S2). The samples were analyzed by means of the ChimeraScan^(S3) algorithm in order to detect a list of gene fusion candidates. Briefly, ChimeraScan detects those reads that discordantly align to different transcripts of the same reference (split inserts). These reads provide an initial set of putative fusion candidates. Finally, the algorithm realigns the initially unmapped reads to the putative fusion candidates and detects those reads that align across the junction boundary (split reads). These reads provide the genomic coordinates of the breakpoint.

RNA-Seq analysis detected a total of 39,329 putative gene fusion events. In order to focus the experimental analysis on biologically relevant fused transcripts, Pegasus annotation pipeline (http://sourceforge.net/projects/pegasus-fus/) were applied. For each putative fusion, Pegasus reconstructs the entire fusion sequence on the base of genomic fusion breakpoint coordinates and gene annotations. Pegasus also annotates the reading frame of the resulting fusion sequences as either in-frame or frame-shift. Moreover, Pegasus detects the protein domains that are either conserved or lost in the new chimeric event by predicting the amino acid sequence and automatically querying the UniProt web service. On the basis of the Pegasus annotation report, relevant gene fusions were selected for further experimental validation according to the reading frame and the conserved/lost domains. The selected list (Table 7) was based on in-frame events expressed by ten or more reads and at least one read spanning the breaking point. To filter out candidate transplicing events, events with putative breakpoints at a distance of at least 25 kb were focused.

EXome-Fuse: Identification of Genetic Rearrangments Using Whole-Exome Data.

Although whole-exome sequencing data contains low intronic coverage that reduces the sensitivity for fusion discovery, it is readily available through the TCGA database. To characterize the genomic breakpoint of the chromosomal rearrangement, EXome-Fuse was designed: a gene fusion discovery pipeline particularly designed to analyze whole-exome data. For the samples harboring EGFR-SEPT14, EGFR-PSPH, NFASC-NTRK1, and BCAN-NTRK1 fusions in RNA, EXome-Fuse was applied to the corresponding whole-exome sequencing data deposited in TCGA. This algorithm can be divided into three stages: split insert identification, split read identification, and virtual reference alignment. Mapping against the human genome reference hg18 with BWA, all split inserts were first identified to compile a preliminary list of fusion candidates. This list was cut of any false positives produced from paralogous gene pairs using the Duplicated Genes Database and the EnsemblCompara GeneTrees⁴. Pseudogenes in the candidate list were annotated using the list from HUGO Gene Nomenclature Committee (HGNC) database^(S5) and given lower priority. Candidates were also filtered out between homologous genes, as well as those with homologous or low-complexity regions around the breakpoint. For the remaining fusion candidates, any supporting split reads and their mates were probed using BLAST with a word size of 16, identity cutoff of 90%, and an expectation cutoff of 10⁻⁴. Finally, a virtual reference was created for each fusion transcript and all reads were re-align to calculate a final tally of split inserts and split reads such that all aligning read pairs maintain F-R directionality.

Targeted Exon Sequencing

All protein-coding exons for the 24 genes of interest were sequenced using genomic DNA extracted from frozen tumors and matched blood. 500 ng of DNA from each sample were sheared to an average of 150 bp in a Covaris instrument for 360 seconds (Duty cycle—10%; intensity—5; cycles/Burst—200). Barcoded libraries were prepared using the Kapa High-Throughput Library Preparation Kit Standard (Kapa Biosystems). Libraries were amplified using the KAPA HiFi Library Amplification kit (Kapa Biosystems) (8 cycles). Libraries were quantified using Qubit Fluorimetric Quantitation (Invitrogen) and the quality and size assessed using an Agilent Bioanalyzer. An equimolar pool of the 4 barcoded libraries (300 ng each) was created and 1,200 ng was input to exon capture using one reaction tube of the custom Nimblegen SeqCap EZ (Roche) with custom probes target the coding exons of the 38 genes. Capture by hybridization was performed according to the manufacturer's protocols with the following modifications: 1 nmol of a pool of blocker oligonucleotides (complementary to the barcoded adapters), and (B) post-capture PCR amplification was done using the KAPA HiFi Library Amplification kit instead of the Phusion High-Fidelity PCR Master Mix with HF Buffer Kit, in a 60 μl volume, since the Kapa HiFi kit greatly reduced or eliminated the bias against GC-rich regions. The pooled capture library was quantified by Qubit (Invitrogen) and Bioanalyzer (Agilent) and sequenced in on an Illumina MiSeq sequencer using the 2×150 paired-end cycle protocol. Reads were aligned to the hg19 build of the human genome using BWA with duplicate removal using samtools as implemented by Illumina MiSeq Reporter. Variant detection was performed using GATK UnifiedGenotyper. Somatic mutations were identified for paired samples using SomaticSniper and filtered for frequency of less than 3% in normal and over 3% in tumor samples. Variants were annotated with Charity annotator to identify protein-coding changes and cross-referenced against known dbSNP, 1000 Genomes, and COSMIC mutations. Sanger sequencing was used to confirm each mutation from normal and tumor DNA.

Modeling of LZTR-1

Structural templates for the Kelch and BTB-BACK regions of human LZTR-1 were identified with HHpred^(S6). An initial 3D model was generated with the I-TASSER server^(S7). The Cul3 N-terminal domain was docked onto the model by superposing the KLHL3^(BTB-BACK)/Cul3^(NTD) crystal structure (PDB ID 4HXI, Xi and Privé PLOS ONE 2013) onto the second LZTR-1 BTB-BACK domain. The model does not include higher quaternary structure, although many BTB domains, and many Kelch domains, are known to self-associate^(S8). The short linkage between the end of the first BACK domain and the beginning of the second BTB domain would appear to preclude an intrachain BTB-BTB pseudo-homodimer; without being bound by theory, LZTR-1 self-associates and forms higher order assemblies. Both BACK domains are the shorter, atypical form of the domain and consist of 2 helical hairpin motifs, as in SPOP^(S9,S10), and not the 4-hairpin motif seen most BTB-BACK-Kelch proteins^(S10,S11). The model from the Kelch domain predicts an unusual 1+3 velcro arrangement^(S12), with the N-terminal region contributing strand d of blade 1 and the C-terminal region contributing strands a,b,c of the same blade, although an alternative 2+2 velcro model cannot be ruled out.

Cell Culture

SNB19 and U87 cells were cultured in DMEM supplemented with 10% Fetal Bovine Serum. Growth rate was determined by plating cells in six-well plates post 3 days after infection with the lentivirus indicated in Figure Legends. The number of viable cells was determined by trypan blue exclusion in triplicate cultures obtained from triplicate independent infections. Migration was evaluated by Confluent cells were scratched with a pipette tip and cultured in 0.25% FBS. After 16 h, images were taken using the Olympus IX70 connected to a digital camera. Images were processed using the ImageJ64 software. The area of the cell-free wound was assessed in triplicate samples. Experiments were repeated twice.

Immunofluorescence and Western Blot

immunoflurescence staining on brain tumor tissue microarrays were performed as previously described^(S17) Immunofluorescence microscopy was performed on cells fixed with 4% para-formaldehyde (PFA) in phosphate buffer. Cells were permeabilized using 0.2% Triton X 100. Antibodies and concentrations used in immunofluorescence staining are:

B-III Tubulin Mouse 1:400 Promega Catenin D2 Guinea Pig 1:500 Acris Fibronectin Mouse 1:1,000 BD-Pharmingen PSD-95 Rabbit 1:500 Invitrogen

Secondary antibodies conjugated to Alexa Fluor 594 (Molecular Probes) were used. DNA was stained by DAPI (Sigma). Fluorescence microscopy was performed on a Nikon A1R MP microscope.

Western blot analysis of U87 cells transduced with pLOC-GFP or pLOC CTNND2 was performed using the following antibodies:

Anti-Vinculin Mouse 1:400 SIGMA Anti-N-Cadherin Mouse 1:200 BD-Pharmingen Cyclin A Rabbit 1:500 Santa Cruz P27 Mouse 1:250 BD Transduction

Cloning and Lentiviral Production

The lentiviral expression vector, pLOC-GFP and pLOC-LZTR1 were purchased from Open Biosystems. The full length EGFR-SEPT14 cDNA was amplified from tumor sample TCGA-27-1837. Primers used were: EGFR FW: 5′-agcgATGCGACCCTCCGGGA-3′ (SEQ ID NO: 30) and SEPT14 REV: 5′-TCTTACGATGTTTGTCTTTCTTTGT (SEQ ID NO: 31); EGFR wild type, EGFR Viii and EGFR-SEPT14 cDNAs were cloned into pLoc and lentiviral particles were produced using published protocols^(S13-S15).

Genomic and mRNA RT-PCR

Total RNA was extracted from cells by using RNeasy Mini Kit (QIAGEN), following the manufacturer instructions. 500 ng of total RNA was retro-transcribed by using the Superscript III kit (Invitrogen), following the manufacturer instructions. The cDNAs obtained after the retro-transcription was used as templates for qPCR as described^(S13,S15). The reaction was performed with a Roche480 thermal cycler, using the Absolute Blue QPCR SYBR Green Mix from Thermo Scientific. The relative amount of specific mRNA was normalized to GAPDH. Results are presented as the mean±SD of triplicate amplifications. The validation of fusion transcripts was performed using both genomic and RT-PCR with forward and reverse primer combinations designed within the margins of the paired-end read sequences detected by RNA-seq. Expressed fusion transcript variants were subjected to direct sequencing to confirm sequence and translation frame. Primers used for the screening of gene fusions are:

hEGFR-RT-FW1: (SEQ ID NO: 32) 5′- GGGTGACTGTTTGGGAGTTGATG -3′; hSEP14-RT-REV1: (SEQ ID NO: 33) 5′- TGTTTGTCTTTCTTTGTATCGGTGC-3′; hEGFR-RT-FW1: (SEQ ID NO: 34) 5′- GTGATGTCTGGAGCTACGGG-3′; hPSPH-RT-REV1: (SEQ ID NO: 35) 5′- TGCCTGATCACATTTCCTCCA-3′; hNFASC-RT-FW1: (SEQ ID NO: 36) 5′- AGTTCCGTGTCATTGCCATCAAC-3′; hNTRK1-RT-REV1: (SEQ ID NO: 37) 5′- TGTTTCGTCCTTCTTCTCCACCG-3′; hCAND1-RT-FW1: (SEQ ID NO: 38) 5′- GGAAAAAATGACATCCAGCGAC-3′; hEGFR-RT-REV1: (SEQ ID NO: 39) 5′- TGGGTGTAAGAGGCTCCACAAG-3′.

Primers used for genomic detection of gene fusions are:

genomic EGFR-FW1: (SEQ ID NO: 40) 5′- GGATGATAGACGCAGATAGTCGCC-3′; genomic SEPT14-REV1: (SEQ ID NO: 41) 5′- TCCAGTTGTTTTTTCTCTTCCTCG-3′; genomic NFASC-FW1: (SEQ ID NO: 42) 5′- AAGGGAGAGGGGACCAGAAAGAAC -3′; genomic NTRK1-REV1: (SEQ ID NO: 43) 5′- GAAAGGAAGAGGCAGGCAAAGAC -3′; genomic CAND1-FW1: (SEQ ID NO: 44) 5′- GCAATAGCAAAACAGGAAGATGTC-3′; genomic EGFR-REV1: (SEQ ID NO: 45) 5′- GAACACTTACCCATTCGTTGG-3′.

Subcutaneous Xenografts and Drug Treatment

Female athymic mice (nu/nu genotype, Balb/c background, 6 to 8 weeks old) were used for all antitumor studies. Patient-derived adult human glioblastoma xenografts were maintained. Xenografts were excised from host mice under sterile conditions, homogenized with the use of a tissue press/modified tissue cytosieve (Biowhitter Inc, Walkersville, Md.) and tumor homogenate was loaded into a repeating Hamilton syringe (Hamilton, Co., Reno, Nev.) dispenser. Cells were injected sub-cutaneously into the right flank of the athymic mouse at an inoculation volume of 50 μl with a 19-gauge needle^(S16). Subcutaneous tumors were measured twice weekly with hand-held vernier calipers (Scientific Products, McGraw, Ill.). Tumor volumes, V were calculated with the following formula: [(width)×(length)]/2=V (mm³) For the sub-cutaneously tumor studies, groups of mice randomly selected by tumor volume were treated with EGFR kinase inhibitors when the median tumor volumes were on average 150 mm³ and were compared with control animals receiving vehicle (saline). Erlotinib was administered at 100 mg/Kg orally daily for 10 days. Lapatinib was administered at 75 mg/Kg orally twice per day for 20 days. Response to treatment was assessed by delay in tumor growth and tumor regression. Growth delay, expressed as T-C, is defined as the difference in days between the median time required for tumors in treated and control animals to reach a volume five times greater than that measured at the start of the treatment. Tumor regression is defined as a decrease in tumor volume over two successive measurements. Statistical analysis was performed using a SAS statistical analysis program, the Wilcoxon rank order test for growth delay, and Fisher's exact test for tumor regression as previously described.

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Example 2 Genomic Alterations in Glioblastoma

Glioblastoma remains one of the most challenging forms of cancer to treat. This example discusses a computational platform that integrates the analysis of copy number variations and somatic mutations and unravels the landscape of in frame gene fusions in glioblastoma. Mutations were found with loss of heterozygosity of LZTR-1, an adaptor of Cul3-containing E3 ligase complexes. Mutations and deletions disrupt LZTR-1 function, which restrains self-renewal and growth of glioma spheres retaining stem cell features. Loss-of-function mutations of CTNND2 target a neural-specific gene and are associated with transformation of glioma cells along the very aggressive mesenchymal phenotype. Recurrent translocations are reported that fuse the coding sequence of EGFR to several partners, with EGFR-SEPT14 as the most frequent functional gene fusion in human glioblastoma. EGFR-SEPT14 fusions activate Stat3 signaling and confer mitogen independency and sensitivity to EGFR inhibition. These results provide important insights into the pathogenesis of glioblastoma and highlight new targets for therapeutic intervention.

Glioblastoma (GBM) is the most common primary intrinsic malignant brain tumor affecting ˜10,000 new patients each year with a median survival rate of 12-15 months^(1,2). Identifying and understanding the functional significance of genetic alterations that drive initiation and progression of GBM is crucial to develop effective therapies. Previous efforts in GBM genome characterization identified somatic changes in well-known GBM genes (EGFR, PTEN, IDH1, TP53, NF1, etc.) and nominated putative cancer genes with somatic mutations, but the functional consequence of most alterations is unknown³⁻⁶. Furthermore, the abundance of passenger mutations and large regions of copy number variations (CNVs) complicates the definition of the landscape of driver mutations in glioblastoma. To address this challenge, a statistical approach was used to nominate driver genes in GBM by integrating somatic mutations identified by whole-exome sequencing with a CNVs analysis that prioritizes focality and magnitude of the genetic alterations.

Recurrent and oncogenic gene fusions are hallmarks of hematological malignancies and have also been uncovered in solid tumors^(7,8). Recently, a small subset of GBM harbor FGFR-TACC gene fusions was reported indicating that the patients with FGFR-TACC-positive tumors would benefit from targeted FGFR kinase inhibition⁹. It remains unknown whether gene fusions involving other RTK-coding genes exist and produce oncogene addiction in GBM. Here, a large RNA-sequencing dataset of primary GBM and Glioma Sphere Cultures (GSCs) is investigated and the global landscape of in frame gene fusions in human GBM are reported.

Nomination of Candidate GBM Genes

Without being bound by theory, integration of somatic point mutations and focal CNVs will uncover candidate driver GBM genes. MutComFocal is an algorithm designed to rank genes by an integrated recurrence, focality and mutation score (see Methods). This strategy was applied to 139 GBM and matched normal DNA analyzed by whole-exome sequencing to identify somatic mutations and 469 GBM analyzed by the Affymetrix SNP6.0 platform to identify CNVs.

The whole-exome analysis revealed a mean of 43 nonsynonymous somatic mutations per tumor sample. The distribution of substitutions shows a higher rate of transitions versus tranversions (67%), with a strong preference for C→T and G→A (55%) (FIG. 6). As seen in other tumor types¹⁰, 19.2% of the mutations occurred in a CpG dinucleotide context (FIG. 7). Among somatic small nucleotide variants, the most frequently mutated genes have roles in cancer, including GBM (TP53, EGFR, PTEN, and IDH1). In addition to known cancer genes, new candidate driver genes were mutated in ˜5% of tumor samples. By integrating mutational and common focal genomic lesions, MutComFocal stratified somatically mutated genes into three groups: recurrently mutated genes without significant copy number alterations (Mut), in regions of focal and recurrent amplifications (Amp-Mut) and in regions of focal and recurrent deletions (Del-Mut).

A list of 67 genes were generated that score at the top of each of the three categories and included nearly all the genes previously implicated in GBM. Among these genes, (labeled in light grey in FIG. 1) are IDH1 (Mut, FIG. 1a ), PIK3C2B, MDM4, MYCN, PIK3CA, PDGFRA, KIT, EGFR, and BRAF (Amp-Mut, FIG. 1b ) and PIK3R1, PTEN, RB1, TP53, NF1 and ATRX (Del-Mut, FIG. 1c ). The analysis also selected 52 new candidate driver genes previously unreported in GBM. Based upon their role in CNS development and homeostasis as well as their potential function in gliomagenesis, 24 genes were selected for re-sequencing in an independent dataset of 83 GBM and matched normal controls. Eighteen genes were found somatically mutated by Sanger sequencing in the independent panel (labeled in dark grey in FIG. 1). Each validated new GBM gene is targeted by somatic mutations and CNVs in a cumulative fraction comprised between 2.9% and 45.7% of GBM. Furthermore, mutations of the 18 new GBM genes occur mostly in tumors with global mutation rates similar to the mean of 43 mutations per tumor and well within the 95% confidence interval, indicating that mutations of the 18 new genes do not cluster in hypermutated tumors (FIG. 2C and FIG. 9).

Among the commonly mutated and focally deleted genes exhibiting top MutComFocal scores and validated in the independent GBM dataset, BCOR, LRP family members, HERC2, LZTR-1 and CTNND2. BCOR, an X-linked gene, encodes for a component of the nuclear co-repressor complex that is essential for normal development of neuroectoderm and stem cell functions¹¹⁻¹³. BCOR mutations have recently been described in retinoblastoma and medulloblastoma^(14,15). LRP1B, a member of the LDL receptor family, is among the most frequently mutated genes in human cancer (FIG. 1c )¹⁶. Interestingly, two other LDL receptor family members (LRP2 and LRP1) are mutated in 4.4% and 2.9% of tumors, respectively (FIG. 1a ). The LRP proteins are highly expressed in the neuroepithelium and are essential for forebrain morphogenesis in mouse and humans^(17,18). The tumor suppressor function of LRP proteins in GBM may relate to the ability to promote chemosensitivity and control in the Sonic hedgehog signaling pathway, which is implicated in cancer initiating cells in GBM¹⁹⁻²¹. Localized on chromosome 15q13, the Hect ubiquitin ligase Herc2 gene is deleted and mutated in 15.1% and 2.2% of GBM cases, respectively. Herc2 has been implicated in severe neurodevelopmental syndromes and Herc2 substrates regulate genome stability and DNA damage-repair^(22,23).

LZTR-1 Mutations Inactivate a Cullin-3 Adaptor to Drive Self-Renewal and Growth of Glioma Spheres

A gene that received one of the highest Del-Mut score by MutComFocal is LZTR-1 (FIG. 1c ). The LZTR-1 coding region had non-synonymous mutations in 4.4%, and the LZTR-1 locus (human chromosome 22q11) was deleted in 22.4% of GBM. Among the 18 new GBM genes, LZTR-1 had the highest co-occurrence score of mutations and deletions (Fisher's exact test, p=0.0007). It also scored at the top of the list of genes whose CNVs are statistically correlated with expression (Pearson correlation between LZTR-1 CNVs and expression is 0.36, p-value<10⁻⁶ by Student's t-distribution). Finally, LZTR-1 emerged as the gene with the highest correlation for monoallelic expression of mutant alleles in tumors harboring LZTR-1 deletions (p-value=0.0007). Taken together, these findings indicate that LZTR-1 is concurrently targeted in GBM by mutations and copy number loss, fulfilling the two-hits model for tumor suppressor inactivation in cancer.

LZTR-1 codes for a protein with a characteristic Kelch-BTB-BACK-BTB-BACK domain architecture (FIGS. 2C, 8, 9) and is expressed in normal brain. The LZTR-1 gene is highly conserved in metazoans. Although it was initially proposed that LZTR-1 functions as a transcriptional regulator, this role was not confirmed in follow-up studies²⁴. Most proteins with BTB-BACK domains are substrate adaptors in Cullin-3 (Cul3) ubiquitin ligase complexes, in which the BTB-BACK region binds to the N-terminal domain of Cul3, while a ligand binding domain, often a Kelch 6-bladed β-propeller motif, binds to substrates targeted for ubiquitylation²⁵. To ask whether LZTR-1 directly binds Cul3, co-immunoprecipitation experiments were performed in human glioma cells. FIG. 15 shows that Cul3 immunoprecipitates contain LZTR-1, indicating that LZTR-1 is an adaptor in Cul3 ubiquitin ligase complexes.

To address the function of LZTR-1 mutants, a homology model of LZTR-1 was built based partly on the crystal structures of the MATH-BTB-BACK protein SPOP²⁶, the BTB-BACK-Kelch proteins KLHL3²⁷ and KLHL11²⁸, and the Kelch domain of Keap1²⁹ (FIG. 2b ). Without being bound by theory, the second BTB-BACK region of LZTR-1 binds Cul3 because of φ-X-E motif in this BTB domain, followed by a 3-Box/BACK region (FIG. 9)²⁶. However, the preceding BTB-BACK region can also participate in Cul3 binding. Five of seven LZTR-1 mutations identified in GBM are located within the Kelch domain and target highly conserved amino acids (FIG. 2b , FIG. 2C, FIG. 8). Interestingly, the concentration of LZTR-1 mutations in the Kelch domain reflects a similar pattern of mutations in the Kelch-coding region of KLHL3, recently identified in families with hypertension and electrolytic abnormalities^(30,31).

The R198G and G248R mutations localize to the b-c loop of the Kelch domain, in a region predicted to provide the substrate-binding surface²⁹. The W105R mutation targets a highly conserved anchor residue in the Kelch repeats and the T288I mutation disrupts a buried residue conserved in LZTR-1 (FIG. 2b , FIG. 2C, FIG. 8). Both mutations are expected to perturb folding of the Kelch domain. The E353STOP mutation is expected to produce a misfolded Kelch domain besides removing the C-terminal BTB-BACK regions. Located in the BTB-BACK domains, the remaining two mutations either truncate the entire BTB-BACK-BTB-BACK region (W437STOP) or are predicted to disrupt the folding of the last helical hairpin in the BTB-BACK domain (R810W, FIG. 2b ).

To ask whether the mutations predicted to affect the BTB-BACK domains perturb the interaction with Cul3, in vitro translated wild type, E353STOP, W437STOP and R810W LZTR-1 Myc-tagged proteins were prepared and their ability to bind to Flag-Cul3 purified from mammalian cells was tested. Wild type LZTR-1 bound Flag-Cul3, but the E353STOP and W437STOP mutants lost this property. However, the R810W mutant retained Cul3 binding in this assay (FIG. 16A). Besides promoting ubiquitin-mediated degradation of substrates, Cullin adaptors are short-lived proteins that undergo auto-ubiquitylation and destruction by the same Cullin complexes that direct substrate ubiquitylation³²⁻³⁴. Thus, impaired ubiquitin ligase activity of the LZTR-1-Cul3 complex should result in accumulation of mutant LZTR-1 proteins. Each of the three LZTR-1 mutants predicted to compromise integrity of the BTB-BACK domains accumulated at higher levels than wild-type LZTR-1 in transient transfection assays (FIG. 16B). The steady state and half-life of the LZTR-1 R810W mutant protein were markedly increased, in the absence of changes of the mutant mRNA (FIG. 16C-D). Thus, as for the two truncated mutants, the R810W mutation compromised protein degradation.

Next, the biological consequences of LZTR-1 inactivation in human GBM. Differential gene expression pattern of GBM harboring mutations was examined and deletions of LZTR-1 or normal LZTR-1 revealed that tumors with genetic inactivation of LZTR-1 were enriched for genes associated with glioma sphere growth and proliferation³⁵ (FIG. 17A). Introduction of LZTR-1 in three independent GBM-derived sphere cultures resulted in strong inhibition of glioma sphere formation and expression of glioma stem cell markers (FIG. 17B-E). LZTR-1 also decreased the size of tumor spheres, induced a flat and adherent phenotype and reduced proteins associated with cell cycle progression (cyclin A, PLK1, p107, FIG. 17D-E). Interestingly, both R810W and W437STOP LZTR-1 mutations abolished LZTR-1 ability to impair glioma sphere formation (FIG. 17F). The above experiments indicate that LZTR-1 inactivation in human GBM drives self-renewal and growth of glioma spheres.

Inactivation of CTNND2 Induces Mesenchymal Transformation in Glioblastoma

Among the top ranking genes in MutComFocal, CTNND2 is expressed at the highest levels in normal brain. CTNND2 codes for δ-catenin, a member of the p120 subfamily of catenins expressed almost exclusively in the nervous system where it is crucial for neurite elongation, dendritic morphogenesis and synaptic plasticity³⁶⁻³⁸. Germ-line hemizygous loss of CTNND2 impairs cognitive functions and underlies some forms of mental retardation^(39,40). CTNND2 shows pronounced clustering of mutations in GBM. The observed spectrum of mutations includes four mutations in the armadillo-coding domain and one in the region coding for the N-terminal coiled-coil domain (FIG. 10A), the two most relevant functional domains of δ-catenin. Each mutation targets highly conserved residues with probably (K629Q, A776T, S881L, D999E) and possibly (A71T) damaging consequences⁴¹. GBM harbors focal genomic losses of CTNND2, and deletions correlate with loss of CTNND2 expression (FIG. 10B).

Immunostaining experiments showed that δ-catenin is strongly expressed in normal brain, particularly in neurons, as demonstrated by co-staining with the neuronal markers β3-tubulin and MAP2 but not the astrocytic marker GFAP (FIG. 18A-B). Conversely, immunostaining of 69 GBM and western blot of 9 glioma sphere cultures revealed negligible or absent expression of δ-catenin in 21 tumors and in most glioma sphere cultures (FIG. 22). Oncogenic transformation in the CNS frequently disrupts the default proneural cell fate and induces an aberrant mesenchymal phenotype associated with aggressive clinical outcome⁴². Gene expression analysis of 498 GBM from ATLAS-TCGA showed that low CTNND2 expression is strongly enriched in tumors exhibiting the mesenchymal gene expression signature (t-test p-value=2.4 10⁻¹², FIG. 10D). Tumors with reduced CTNND2 were characterized by poor clinical outcome and, among them, tumors with CTNND2 copy number loss displayed the worst prognosis (FIG. 3C-D). Patients with low CTNND2 expression showed the worst clinical outcome in mesenchymal GBM, though non-mesenchymal tumors also demonstrated poor prognosis, albeit with reduced strength (FIG. 3D).

Mesenchymal transformation of GBM is associated with irreversible loss of proneural cell fate and neuronal markers⁴² and is detected in most established glioma cell lines. Expression of δcatenin in the U87 human glioma cell line reduced cell proliferation (FIG. 3E), elevated expression of neuronal proteins βIII-tubulin, PSD95 (a post-synaptic marker) and N-cadherin (FIG. 3G, FIG. 23A) and decreased mRNA and protein levels of mesenchymal markers (FIG. 3F, FIG. 18C, FIG. 23A). These effects were associated with morphologic changes characterized by neurite extension and development of branched dendritic processes (FIG. 3F, FIG. 23B-23C). Conversely, expression of the A776T, K629Q and D999E mutants of CTNND2 failed to induce neuronal features and down-regulate the mesenchymal marker fibronectin (FBN, FIG. 18C, FIG. 23B-23C). Consistent with 8-catenin inhibition of cell proliferation in glioma cells, only wild type δ-catenin decreased cyclin A, a S-phase cyclin (FIG. 18C).

Next, the effect of expressing δ-catenin in GBM-derived sphere culture #48 that lacks the endogenous δ-catenin protein (FIG. 22B) and expresses high levels of mesenchymal markers was analyzed⁴³. Introduction of δ-catenin in sphere culture #48 strongly reduced mesenchymal proteins smooth muscle actin (SMA), collagen-5A1 (Col5A1) and FBN, as measured by quantitative immunofluorescence (FIGS. 19A-B). It also induced βIII-tubulin more than eight-fold (FIGS. 19C-D). Time course analysis showed the highest degree of βIII-tubulin-positive neurite extension at 4-6 days post-transduction followed by progressive depletion of neuronal-like cells from culture (FIG. 19D). Finally, whether 8-catenin impacts self-renewal and growth of glioma spheres in vitro and their ability to grow as tumor masses in vivo were examined. In a limiting dilution assay, δ-catenin inhibited glioma sphere formation more than 8-fold (FIG. 19E). To determine the effect of δ-catenin on brain tumorigenesis in vivo, #48 glioma sphere cultures were generated expressing luciferase and bioluminescence imaging was conducted at different times after stereotactic transduction of control and δ-catenin-expressing cells in the mouse brain. When compared to controls, a 5-fold inhibition of tumor growth by δ-catenin at each time point analyzed (FIG. 19F, FIG. 23D). These results identify CTNND2 inactivation as a key genetic alteration driving the aggressive mesenchymal phenotype of GBM.

Recurrent EGFR Fusions in GBM

To identify gene fusions in GBM, RNA-seq data was analyzed from a total of 185 GBM samples (161 primary GBM plus 24 short-term glioma sphere cultures freshly isolated from patients carrying primary GBM). The analysis of RNA-seq led to the discovery of 92 candidate rearrangements giving rise to in-frame fusion transcripts (Table 7). Besides previously reported FGFR3-TACC3 fusions events, the most frequent recurrent in-frame fusions involved EGFR in 7.6% of samples (14/185, 3.8%-11.3% CI). Nine of 14 EGFR fusions included recurrent partners SEPT14 (6/185, 3.2%) and PSPH (3/185, 1.6%) as the 3′ gene segment in the fusion. All EGFR-SEPT14 and two of three EGFR-PSPH gene fusions occurred within amplified regions of the fusion genes (FIG. 24).

The quantitative analysis of expressed reads spanning the fusion breakpoint versus reads spanning EGFR exons not implicated in the fusion transcripts revealed that EGFR fusion genes were expressed at higher levels in five of nine tumors (Table 11). Two in-frame highly expressed fusions involving the neurotrophic tyrosine kinase receptor 1 gene (NTRK1) as the 3′ gene with two different 5′ partners (NFASC-NTRK1 and BCAN-NTRK1). Fusions involving NTRK1 are common in papillary thyroid carcinomas⁴⁴. Using EXomeFuse, an algorithm that reconstructs genomic fusions from whole-exome data, EGFR-SEPT14 and NRTK1 fusions result from recurrent chromosomal translocations and the corresponding genomic breakpoints were reconstructed (Table 12).

The sequence of the PCR products spanning the fusion breakpoint validated all three types of recurrent in frame fusion predictions (EGFR-SEPT14, EGFR-PSPH and NRTK1 fusions, FIGS. 4, 11, 12). In FIGS. 4A-B, the prediction and cDNA sequence validation is shown respectively, for one tumor harboring an EGFR-SEPT14 fusion (TCGA-27-1837). The amplified cDNA contained an open reading frame for a 1,041 amino-acid protein resulting from the fusion of EGFR residues 1-982 with SEPT14 residues 373-432 (FIG. 4C). Thus, the structure of EGFR-Septin14 fusions involves EGFR at the N-terminus, providing a receptor tyrosine kinase domain fused to a coiled-coil domain from Septin14. Exon-specific RNA-seq expression in TCGA-27-1837 demonstrated that EGFR and SEPT14 exons implicated in the fusion are highly expressed compared with mRNA sequences not included in the fusion event (FIG. 13).

Using PCR, the genomic breakpoint was mapped to chromosome 7 (#55,268,937 for EGFR and #55,870,909 for SEPT14, genome build GRCh37/hg19) within EGFR exon 25 and SEPT14 intron 9, creating a transcript in which the 5′ EGFR exon 24 is spliced to the 3′ SEPT14 exon 10 (FIG. 4D). Interestingly, the fused EGFR-PSPH cDNA and predicted fusion protein in sample TCGA-06-5408 involves the same EGFR N-terminal region implicated in the EGFR-SEPT14 with PSPH providing a carboxy-terminal portion of 35 amino acids (FIG. 11). An example of a fusion in which the EGFR-TK region is the 3′ partner is the CAND1-EGFR fusion in the glioma sphere culture #16 (FIG. 14). Each fusion transcript includes the region of the EGFR mRNA coding for the TK domain (Table 7). RT-PCR and genomic PCR followed by Sanger sequencing of GBM TCGA-06-5411 validated the NFASC-NTRK1 fusions in which the predicted fusion protein includes the TK domain of the high-affinity NGF receptor (TrkA) fused downstream to the immunoglobulin-like region of the cell adhesion and ankyrin-binding region of neurofascin (FIG. 12).

To confirm that GBM harbors recurrent EGFR fusions and determine the frequency in an independent dataset, cDNA was screened from a panel of 248 GBMs and discovered 10 additional cases with EGFR-SEPT14 fusions (4%). Conversely, NFASC-NTRK1 fusions were not detected in this dataset. A 2.2% (3/135) frequency of EGFR-PSPH fusions was determined.

The discovery of recurrent EGFR fusions in GBM is of particular interest. EGFR is activated in a significant fraction of primary GBM (˜25%) by an in-frame deletion of exons 2-7 (EGFRvIII)⁴⁵. However, seven of nine tumors harboring EGFR-SEPT14 and EGFR-PSPH gene fusions lacked the EGFRvIII rearrangement (Table 13). It was determined whether the most frequent EGFR fusion in GBM (EGFR-SEPT14) provides an alternative mechanism of EGFR activation and confers sensitivity to EGFR inhibition. First, whether EGFR gene fusions cluster into any gene expression subtype of GBM (proneural, neural, classical, mesenchymal) was investigated. Although no individual subtype displayed a statistically significant enrichment of EGFR fusions, 8 of 9 GBM harboring EGFR-SEPT14 or EGFR-PSPH belonged to the classical or mesenchymal subtype (Fisher's P value=0.05 for classical/mesenchymal enrichment, Table 14).

Next, the effects of ectopic EGFR-SEPT14, EGFRvIII or EGFR wild type on glioma cells were investigated. Lentiviral transduction of #48 human glioma sphere culture (which lacks genomic alteration of EGFR) showed that cells expressing EGFR-SEPT14 or EGFRvIII but not those expressing wild type EGFR or vector retained growth and self-renewal in the absence of EGF and bFGF (FIG. 20A). Accordingly, established glioma cell lines expressing EGFR-SEPT14 or EGFRvIII proliferated at higher rate than control cells or cells expressing wild type EGFR (FIG. 5A, FIG. 25). Furthermore, EGFR-SEPT14 and EGFRvIII markedly enhanced migration of glioma cells in a wound assay (FIG. 5B-C). The above findings indicate that EGFR-SEPT14 might constitutively activate signaling events downstream of EGFR. When analyzed in the presence and absence of mitogens, the expression of EGFR-SEPT14 (or EGFRvIII) in glioma sphere cultures #48 triggered constitutive activation of phospho-STAT3 but had no effects on phospho-ERK and phospho-AKT (FIG. 20B-C). This is consistent with enrichment of STAT3-target genes in primary human GBM harboring EGFR-SEPT14 fusions compared with tumors carrying wild type EGFR (FIG. 20D). Differential gene expression analysis identified a set of 9 genes up-regulated in EGFR-SEPT14 tumors compared with EGFRvIII-positive GBM (FIG. 26). These genes broadly relate to inflammatory/immune response, and some code for chemokines (CXCL9, 10, 11) that have been associated with aggressive glioma phenotypes⁴⁶.

Finally, it was investigated whether EGFR-SEPT14 fusions confer sensitivity to inhibition of EGFR-TK. Treatment of #48 expressing EGFR-SEPT14, EGFRvIII, wild type EGFR or vector control with lapatinib, an irreversible EGFR inhibitor recently proposed to target EGFR alterations in GBM⁴⁷, revealed that EGFR-Sept14 and EGFRvIII but not wild-type EGFR sensitized glioma cells to pharmaceutical EGFR inhibition (FIG. 20E). Similar effects were obtained following treatment of #48-derivatives with erlotinib, another inhibitor of EGFR-TK (FIG. 5D).

To ask whether sensitivity to EGFR-TK inhibition is retained in human glioma cells naturally harboring EGFR-SEPT14 in vivo, an EGFR-SEPT14-positive GBM xenograft (D08-0537 MG) established from a heavily pretreated patient was used. Treatment of D08-0537 MG tumors with lapatinib or erlotinib showed that both drugs significantly delayed tumor growth, with lapatinib displaying the strongest anti-tumor effects. Conversely, EGFR inhibitors were ineffective against GBM xenograft D08-0714 MG, which lacks EGFR genomic alterations (FIG. 5E). Taken together, these data determine that EGFR-SEPT14 fusions confer mitogen-independent growth, constitutively activate STAT3 signaling and impart sensitivity to EGFR kinase inhibition to glioma cells harboring the fusion gene.

Discussion

A computational pipeline was described that computes frequency, magnitude and focality of CNVs at any loci in the human genome with the somatic mutation rate for genes residing at that genomic location, thus integrating into a single score two genetic hallmarks of driver cancer genes (focality of CNVs and point mutations). Besides recognizing nearly all genes known to have functional relevance in GBM, this study discovered and validated somatic mutations in 18 new genes, which also harbor focal and recurrent CNVs in a significant fraction of GBM. The importance of some of these genes extends beyond GBM, as underscored by cross-tumor relevance (e.g. BCOR), and protein family recurrence (e.g. LRP family members).

Also, the LZTR-1 mutations targeting highly conserved residues in the Kelch domain (W105, G248, T288) and in the second BTB-BACK domain (R810) are recurrent events in other tumor types⁴⁸. Thus, understanding the nature of substrates of LZTR-1-Cul3 ubiquitin ligase activity will provide important insights into the pathogenesis of multiple cancer types. The importance of LZTR-1 genetic alterations in GBM is underscored by concurrent targeting of LZTR-1 by mutations and deletions that supports a two-hits mechanism of tumor suppressor gene inactivation as well as the impact of mutations targeting the BTB-BACK domains on Cul3 binding and/or protein stability, and their ability to release glioma cells from the restraining activity of the wild-type protein on self-renewal.

The finding that loss-of-function of CTNND2 cluster in mesenchymal GBM provides a clue to the genetic events driving this aggressive GBM subtype. The function of 8-catenin for crucial neuronal morphogenesis indicates that full-blown mesenchymal transformation in the brain requires loss of master regulators constraining cell determination along the neuronal lineage. Introduction of δ-catenin in human glioma spheres collapsed the mesenchymal phenotype and inhibited sphere formation and tumor growth. Thus, the ability of δ-catenin to reprogram glioma cells expressing mesenchymal genes towards a neuronal fate unravels an unexpected plasticity of mesenchymal GBM that might be exploited therapeutically.

In this study, the landscape of gene fusions from a large dataset of GBM analyzed by RNA-Sequencing is also reported. In-frame gene fusions retaining the RTK-coding domain of EGFR emerged as the most frequent gene fusion in GBM. In this tumor, EGFR is frequently targeted by focal amplications and our finding underscores the strong recombinogenic probability of focally amplified genes, as recently reported for the myc locus in medulloblastoma⁴⁹. Resembling intragenic rearrangements that generate the EGFRvIII allele, EGFR-SEPT14 fusions impart to glioma cells the ability to self-renew and grow in the absence of mitogens, constitutively activate STAT3 signaling, and confer sensitivity to EGFR inhibition. These findings highlight the relevance of fusions implicating RTK-coding genes in the pathogenesis of GBM⁹. They also provide a strong rationale for the inclusion of GBM patients harboring EGFR fusions in clinical trials based on EGFR inhibitors.

Methods

SAVI (Statistical Algorithm for Variant Frequency Identification).

The frequencies of variant alleles were estimated in 139 paired tumor and normal whole-exome samples from TCGA using the SAVI pipeline⁵⁰. The algorithm estimates the frequency of variant alleles by constructing an empirical Bayesian prior for those frequencies, using data from the whole sample, and obtains a posterior distribution and high credibility intervals for each allele⁵⁰. The prior and posterior are distributed over a discrete set of frequencies with a precision of 1% and are connected by a modified binomial likelihood, which allows for some error rate. More precisely, a prior distribution p(f) of the frequency f and a prior for the error e uniform on the interval [0,E] for a fixed 0≦E≦1 is assumed. The sequencing data at a particular allele is a random experiment producing a string of m (the total depth at the allele) bits with n ‘1’s (the variant depth at the allele). Assuming a binomial likelihood of the data and allowing for bits being misread because of random errors, the posterior probability P(f) of the frequency f is

${P(f)} = {{\frac{p(f)}{C} \cdot \frac{1}{b - 1}}{\int_{f}^{f + E - {2{Ef}}}{{x^{n}\left( {1 - x} \right)}^{m - n}{x}}}}$

where C is a normalization constant. For a particular allele, the value of E is determined by the quality of the nucleotides sequenced at that position as specified by their Phred scores. The SAVI pipeline takes as input the reads produced by the sequencing technology, filters out low-quality reads and maps the rest onto a human reference genome. After mapping, a Bayesian prior for the distribution of allele frequencies for each sample is constructed by an iterative posterior update procedure starting with a uniform prior. To genotype the sample, the posterior high-credibility intervals were used for the frequency of the alleles at each genomic location. Alternatively, combining the Bayesian priors from different samples, posterior high-credibility intervals were obtained for the difference between the samples of the frequencies of each allele. Finally, the statistically significant differences between the tumor and normal samples are reported as somatic variants. To estimate the positive prediction value of SAVI in the TCGA GBM samples, 41 mutations were selected for independent validation by Sanger sequencing. 39 of the 41 mutations using Sanger sequencing were confirmed, resulting in a 0.95 (95% CI 0.83-0.99) validation rate.

Candidate genes were ranked by the number of somatic nonsynonymous mutations. A robust fit of the ratio of nonsynonymous to synonymous mutations was generated with a bisquare weighting function. The excess of nonsynonymous alterations was estimated using a Poisson distribution with a mean equal to the product of the ratio from the robust fit and the number of synonymous mutations. Genes in highly polymorphic genomic regions were filtered out based on an independent cohort of normal samples. The list of these regions includes families of genes known to generate false positives in somatic predictions (for example, the HLA, KRT and OR gene families).

MutComFocal.

Key cancer genes are often amplified or deleted in chromosomal regions containing many other genes. Point mutations and gene fusions, conversely, provide more specific information about which genes may be implicated in the oncogenic process. MutComFocal was developed, a Bayesian approach that assigns a driver score to each gene by integrating point mutations and CNV data from 469 GBMs (Affymetrix SNP6.0). In general, MutComFocal uses three different strategies. First, the focality component of the score is inversely proportional to the size of the genomic lesion to which a gene belongs and thus prioritizes more focal genomic lesions. Second, the recurrence component of the MutComFocal score is inversely proportional to the total number of genes altered in a sample, which prioritizes samples with a smaller number of altered genes. Third, the mutation component of the score is inversely proportional to the total number of genes mutated in a sample, which achieves the twofold goal of prioritizing mutated genes on one hand and prioritizing samples with a smaller number of mutations on the other.

More specifically, for a particular sample, let (c₁, N₁), . . . , (c_(k), N_(k)) describe the amplification lesions in that sample so that N₁ is the number of genes in the ith lesion and c₁ is its copy number change from normal. For a gene belonging to the ith lesion, the amplification recurrence sample score is defined as (c₁, N₁), . . . , (c_(k), N_(k)), and its amplification focality sample score is defined as (c_(i)/Σ_(j)c_(j))×(1/N_(i)). To obtain the amplification recurrence and focality scores for a particular gene, the corresponding sample scores were summed over all the samples and the result was normalized so that each score sums to 1. The deletion and recurrence scores are defined in a similar manner. The mutation score is analogous to a recurrence score in which it is assumed that mutated genes belong to lesions with only one gene.

The amplification/mutation score is defined as the product of the two amplification scores and the mutation score, whereas the deletion/mutation score is defined as the product of the two deletion scores and the mutation score. The amplification/mutation and deletion/mutation scores are normalized to 1, and for each score, genes are divided into tiers iteratively so that the top 2^(X) remaining genes are included in the next tier, where H is the entropy of the scores of the remaining genes normalized to 1. On the basis of their tier across the different types of scores, genes are assigned to being either deleted/mutated or amplified/mutated, and genes in the top tiers are grouped into contiguous regions. The top genes in each region are considered manually and selected for further functional validation.

The recurrence and focality scores can be interpreted as the posterior probabilities that a gene is driving the selection of the disease under two different priors, one global and one local in nature. The recurrence score is higher if a gene participates in many samples that do not have too many altered genes, whereas the focality score is higher if the gene participates in many focal lesions. Besides lending strong support to the inference of a gene as a potential driver, the directionality of the copy number alteration (amplification or deletion) informs the probable behavior of the candidate gene as an oncogene or tumor suppressor, respectively.

The genes displayed in FIG. 1 were selected on the basis of the MutComFocal ranking (top 250 genes), the size of the minimal region (less than 10 genes) and the frequency of mutations (more than 2% for deletion/mutations and at least 1% for amplification/mutations).

RNA-Seq Bioinformatics Analysis.

161 RNA-seq GBM tumor samples were analyzed from TCGA, a public repository containing large-scale genome sequencing of different cancers, plus 24 patient-derived GSCs. Nine GSC samples reported in previous studies were kept in our analysis to evaluate recurrence⁹. The samples were analyzed using the ChimeraScan⁵¹ algorithm to detect a list of gene fusion candidates. Briefly, ChimeraScan detects those reads that discordantly align to different transcripts of the same reference (split inserts). These reads provide an initial set of putative fusion candidates. The algorithm then realigns the initially unmapped reads to the putative fusion candidates and detects those reads that align across the junction boundary (split reads). These reads provide the genomic coordinates of the breakpoint.

RNA-seq analysis detected a total of 39,329 putative gene fusion events. To focus the experimental analysis on biologically relevant fused transcripts, the Pegasus annotation pipeline (http://sourceforge.net/projects/pegasus-fus/) was applied. For each putative fusion, Pegasus reconstructs the entire fusion sequence on the basis of the genomic fusion breakpoint coordinates and gene annotations. Pegasus also annotates the reading frame of the resulting fusion sequences as either in frame or a frame shift. Moreover, Pegasus detects the protein domains that are either conserved or lost in the new chimeric event by predicting the amino acid sequence and automatically querying the UniProt web service. On the basis of the Pegasus annotation report, relevant gene fusions were selected for further experimental validation according to the reading frame and the conserved and lost domains. The selected list was based on in-frame events expressed by ten or more reads, with at least one read spanning the breaking point. To filter out candidate trans-splicing events, events with putative breakpoints at a distance of at least 25 kb were pursued.

Identification of Genetic Rearrangements Using Whole-Exome Data.

Although whole-exome sequencing data contain low intronic coverage that reduces the sensitivity for fusion discovery, they are readily available through the TCGA database. To characterize the genomic breakpoint of the chromosomal rearrangement, EXome-Fuse, a new gene fusion discovery pipeline that is designed particularly to analyze whole-exome data, was designed. For the samples harboring EGFR-SEPT14, EGFR-PSPH, NFASC-NTRK1 and BCAN-NTRK1 fusions in RNA, EXome-Fuse was applied to the corresponding whole-exome sequencing data deposited in TCGA. This algorithm can be divided into three stages: split-insert identification, split-read identification and virtual reference alignment. Mapping against the human genome reference hg18 with BWA, all split inserts are first identified to compile a preliminary list of fusion candidates. This list was pruned of any false positives produced from paralogous gene pairs using the Duplicated Genes Database and the EnsemblCompara GeneTrees⁵². Pseudogenes in the candidate list were annotated using the list from the HUGO Gene Nomenclature Committee (HGNC) database⁵³ and were given lower priority. Candidates were also filtered out between homologous genes, as well as those with homologous or low-complexity regions around the breakpoint. For the remaining fusion candidates, any supporting split reads were probed for and their mates using BLAST with a word size of 16, identity cutoff of 90% and an expectation cutoff of 10⁻⁴. A virtual reference was created for each fusion transcript and all reads were realigned to calculate a final tally of split inserts and split reads such that all aligning read pairs maintain forward-reverse directionality.

Targeted Exon Sequencing.

All protein-coding exons for the 24 genes of interest were sequenced using genomic DNA extracted from frozen tumors and matched blood. Five-hundred nanograms of DNA from each sample were sheared to an average size of 150 bp in a Covaris instrument for 360 s (duty cycle, 10%; intensity, 5; cycles per burst, 200). Bar-coded libraries were prepared using the Kapa High-Throughput Library Preparation Kit Standard (Kapa Biosystems). Libraries were amplified using the KAPA HiFi Library Amplification kit (Kapa Biosystems) (eight cycles). Libraries were quantified using Qubit Fluorimetric Quantitation (Invitrogen), and the quality and size was assessed using an Agilent Bioanalyzer. An equimolar pool of the four bar-coded libraries (300 ng each) was created, and 1,200 ng was input to exon capture using one reaction tube of the custom Nimblegen SeqCap EZ (Roche) with custom probes targeting the coding exons of the 38 genes. Capture by hybridization was performed according to the manufacturer's protocols with the following modifications: 1 nmol of a pool of blocker oligonucleotides (complementary to the bar-coded adapters) was used, and post-capture PCR amplification was done using the KAPA HiFi Library Amplification kit, instead of the Phusion High-Fidelity PCR Master Mix with HF Buffer Kit, in a 60 μl volume, as the Kapa HiFi kit greatly reduced or eliminated the bias against GC-rich regions.

The pooled capture library was quantified by Qubit (Invitrogen) and Bioanalyzer (Agilent) and sequenced in on an Illumina MiSeq sequencer using the 2×150 paired-end cycle protocol. Reads were aligned to the hg19 build of the human genome using BWA with duplicate removal using SAMtools as implemented by Illumina MiSeq Reporter. Variant detection was performed using GATK UnifiedGenotyper. Somatic mutations were identified for paired samples using SomaticSniper and filtered for frequency of less than 3% in normal samples and over 3% in tumor samples. Variants were annotated with the Charity annotator to identify protein-coding changes and cross referenced against known dbSNP, 1000 Genomes and COSMIC variants. Sanger sequencing was used to confirm each mutation from normal and tumor DNA.

Enrichment of Amplified and Deleted Genes for Single-Nucleotide Variants (SNVs).

Although MutComFocal combines SNV and CNV data to identify genes driving oncogenesis, it does not explicitly determine whether amplified or deleted genes are enriched for SNVs within the same sample. Deletions and SNVs of a gene within the same sample might indicate a two-hit model of a tumor suppressor. Alternatively, amplifications and gain-of-function mutations of an oncogene within the sample might further promote oncogenesis. For each MutComFocal candidate gene, the number of TCGA samples was determined with both amplification and SNVs, amplification alone, SNVs alone or neither. The corresponding Fisher's P value was calculated. A similar analysis for deletions was performed.

Correlation Between Copy Number and Expression.

One method of assessing the functional relevance of an amplified or deleted gene is to assess the effect of gene dosage. For each gene nominated by MutComFocal, the Pearson's correlation coefficient was calculated between copy number and expression. The corresponding P values were computed using paired Student's t test.

Allele-Specific Expression of SNVs.

For a given gene nominated by MutComFocal, RNA sequencing can determine whether the mutant or wild-type allele is expressed. Toward this end, VCFtools54 was applied to the TCGA BAM RNA-seq files produced by TopHat, which produces the depth of reads calling the reference (R) and variant (V) allele. A measure of relative expression of the variant allele is then V/(V+R). For each mutation, the binomial P value of observing more than V out of V+R reads was calculated, assuming that it is equally probable for a read to call the variant or reference. The binomial P values of each mutation were then pooled using the Stouffer's Z-score method to calculate the combined P value per gene.

Ruling Out Passenger Mutations in Hypermutated Samples.

To rule out the possibility that MutComFocal candidates tend to be passenger mutations in hypermutated samples, the number of mutations was compared in samples harboring a MutComFocal mutation to the distribution N of the number of mutations in each TCGA sample. Because the number of TCGA samples was well above 30, N was assummed to be well approximated by the normal distribution and calculated the mean, μ, and s.d., σ. For each MutComFocal mutation, the Z-test was performed and all mutations failed statistical significance after correction by the Benjamini-Hochberg method.

Determining the Presence of EGFRvIII Transcripts.

To determine the prevalence of EGFRvIII transcripts, an in-house script was created to calculate the number of split inserts and split reads supporting the junction between EGFR exons 1 and 8. The EGFRvIII isoform was considered to be expressed if there were more than five split reads or five split inserts in a sample.

Calculating the Relative Expression of EGFR Fusions Compared to Wild-Type EGFR.

To determine the functional relevance of EGFR-SEPT14 and EGFR-PSPH fusions, the relative expression was determined between the fusion and wild-type transcripts within each sample on the basis of BAM files mapped by TopHat and provided by TCGA. As a proxy for expression of the transcript, the depth of reads covering either a mutant or wild-type junction was calculated. In particular, the depth of reads covering the fusion breakpoint of EGFR-SEPT14 or EGFR-PSPH was considered to estimate the expression of the fusion transcript. Because all EGFR fusions stereotypically involved exon 24 joined to either SEPT14 or PSPH, the depth of reads covering the junctions between EGFR exons 25-26, 26-27 and 27-28 to be a specific gauge of wild-type EGFR expression was assessed.

Enrichment of the Classical and Mesenchymal Subtype Among Samples with EGFR Fusions.

To assess whether samples with EGFR fusions tended to occur in a particular GBM subtype, each TCGA GBM sample was first classified by expression according to the methods of Verhaak et al.⁶. The number of classical, mesenchymal, proneural and neural samples was then tallied with and without EGFR gene fusions. The combined class of classical and mesenchymal phenotype was enriched for EGFR fusions according to the Fisher's exact test.

Copy Number Variation in EGFR Fusions.

Gene fusions often arise from genomic instability. Motivated by this observation, segmented SNP array data was downloaded from TCGA and calculated the log 2 ratio between the tumor and normal copy numbers. This was plotted along the chromosomal neighborhood of EGFR, SEPT14 and PSPH (chr7:55,000,000-56,500,000).

GSEA.

To determine the biological impact of LZTR1 mutations, GSEA⁵⁵ was used, which is an analytical tool that harnesses expression data to nominate gene sets enriched for a particular phenotype. Having identified TCGA samples with LZTR1 SNVs, GSEA was applied to the TCGA expression data. Samples were first compared with LZTR1 SNVs against those with wild-type LZTR1 (excluding LZTR1 deletions). To assess statistical significance, the data set was randomized by permuting gene sets 500 times and considered only gene sets with an FDR q<0.05.

Differential Expression Between Samples with EGFR-SEPT14 and EGFRvIII.

In-house differential expression analysis was also performed to determine a distinct molecular signature distinguishing the EGFR-SEPT14 and EGFRvIII phenotypes. Toward this end, a t test was performed comparing the expression of the two groups of samples for each gene. Correcting using the Benjamini-Hochberg method, only genes with FDR<0.05 were considered. In addition, genes were excluded with a variance less than the tenth percentile or absolute value lower than two across all samples. These filters left a predictive set of ten genes. Hierarchical clustering was then performed on the expression of these ten genes using Euclidean distance and average linkage.

Modeling of LZTR1.

Structural templates for the kelch and BTB-BACK regions of human LZTR1 were identified with HHpred⁵⁶. An initial three-dimensional model was generated with the I-TASSER server⁵⁷. The CUL3 N-terminal domain was docked onto the model by superposing the KLHL3^(BTB-BACK)/CUL3^(NTD) crystal structure²⁷ onto the second LZTR1 BTB-BACK domain. The model does not include higher quaternary structure, although many BTB domains, and many kelch domains, are known to self associate²⁵. The short linkage between the end of the first BACK domain and the beginning of the second BTB domain would seem to preclude an intrachain BTB-BTB pseudo-homodimer, and without being bond by theory, LZTR1 should self associate and form higher-order assemblies. Both BACK domains are the shorter, atypical form of the domain and consist of two helical hairpin motifs, as in SPOP^(26,58), and not the four-hairpin motif seen in most BTB-BACK-kelch proteins^(28,58). The model from the kelch domain predicts an unusual 1+3 velcro arrangement⁵⁹, with the N-terminal region contributing strand d of blade 1 and the C-terminal region contributing strands a, b and c of the same blade, although an alternative 2+2 velcro model cannot be ruled out.

Cell Culture.

U87 cells were obtained from ATCC. SNB19, U87 and HEK-293T cells were cultured in DMEM supplemented with 10% fetal bovine serum (FBS). Growth rates were determined by plating cells in six-well plates at 3 d after infection with the lentivirus indicated in the figure legends. The number of viable cells was determined by Trypan blue exclusion in triplicate cultures obtained from triplicate independent infections. For the wound assay testing migration, confluent cells were scratched with a pipette tip and cultured in 0.25% FBS. After 16 h, images were taken using the Olympus IX70 connected to a digital camera. Images were processed using the ImageJ64 software. The area of the cell-free wound was assessed in triplicate samples. Experiments were repeated twice.

GBM-derived primary cultures were grown in DMEM:F12 medium containing N2 and B27 supplements and human recombinant FGF-2 and EGF (50 ng/ml each; Peprotech). For sphere formation, cells were infected with lentiviral particles. Four days later, single cells were plated at density of 1 cells per well in triplicate in low-attachment 96-well plates. The number and the size of spheres were scored after 10-14 d. Limiting dilution assays were performed as described previously⁶⁰. Spheres were dissociated into single cells and plated in low-attachment 96-well plates in 0.2 ml of medium containing growth factors (EGF and FGF-2), except for the EGFR-transduced cells, which were cultured in the absence of EGF. Cultures were left undisturbed for 10 d, and then the percentage of wells not containing spheres for each cell dilution was calculated and plotted against the number of cells per well. Linear regression lines were plotted, and the number of cells required to generate at least one sphere in every well (the stem cell frequency) was calculated. The experiment was repeated twice. Treatment of GBM primary cultures with erlotinib or lapatinib was performed in cells transduced with the pLOC vector, wild-type pLOC-EGFR, EGFRvIII or EGFR-SEPT14 and selected with blasticidin for 5 d. Cells were seeded on 6-cm dishes in the absence of EGF and treated with the indicated drugs at the indicated doses for 48 h. Each treatment group was seeded in triplicate. Absolute viable cell counts were determined by Trypan blue exclusion and counted on a hemocytometer. EGF stimulation of EGFR-transduced primary glioma cells was performed in cells deprived of growth factors for 48 h. Cells were collected at the indicated times and processed for protein blot analysis.

Immunofluorescence.

Immunofluorescence staining on normal mouse and human brain and brain tumor tissue microarrays were performed as previously described^(43,61,62). Immunofluorescence microscopy was performed on cells fixed with 4% paraformaldehyde in phosphate buffer. Cells were permeabilized using 0.2% Triton X-100. The antibodies and concentrations used in the immunofluorescence staining are detailed in Table 15.

Secondary antibodies conjugated to Alexa Fluor 594 (1:300, A11037, Molecular Probes) or Alexa 488 (1:500, A11008, Molecular Probes) were used. DNA was stained with DAPI (Sigma). Fluorescence microscopy was performed on a Nikon A1R MP microscope. Quantification of the fluorescence intensity staining in primary or established glioma cells was performed using NIH ImageJ software (see URLs). A histogram of the intensity of fluorescence of each point of a representative field for each condition was generated. The fluorescence intensity of ten fields from three independent experiments was scored, standardized to the number of cells in the field and divided by the intensity of the vector.

Protein Blotting, Immunoprecipitation and In Vitro Binding.

Protein blot analysis and immunoprecipitation were performed using the antibodies detailed in Table 16. For the in vitro binding between CUL3 and LZTR1, wild-type and mutant LZTR1 were translated in vitro using the TNT Quick Coupled Transcription/Translation System (Promega). Flag-CUL3 was immunoprecipitated from transfected HEK-293T cells with Flag-M2 beads (Sigma) using RIPA buffer (50 mM Tris-HCl, pH 7.5, 150 mM NaCl, 1% NP-40, 0.5% sodium deoxycholate (DOC), 0.1% SDS, 1 mM phenylmethylsulfonyl fluoride (PMSF), 10 mM NaF, 0.5 M Na₃OV₄ (sodium orthovanadate) and Complete Protease Inhibitor Cocktail, Roche). Binding was performed in 200 mM NaCl plus 0.5% NP-40 for 2 h at 4° C. Immunocomplexes were analyzed by SDS-PAGE and immunoblot.

Cloning and Lentiviral Production.

The lentiviral expression vectors pLOC-GFP and pLOC-CTNND2 were purchased from Open Biosystems. Full-length EGFR-SEPT14 cDNA was amplified from tumor sample TCGA-27-1837. Wild-type EGFR, EGFRvIII and EGFR-SEPT14 cDNAs were cloned into the pLOC vector. pCDNA-MYC-Hist-LZTR1 was a kind gift²⁴. pCDNA-Flag-CUL3 was a gift. Wild-type and mutant cDNAs for LZTR1 and CTNND2 obtained by site-directed mutagenesis (QuikChange II, Agilent) were cloned into the pLOC vector. Lentiviral particles were produced using published protocols^(43, 61, 62, 63, 64).

Genomic PCR and RT-PCR.

Total RNA was extracted from cells using an RNeasy Mini Kit (QIAGEN) following the manufacturer's instructions. Five-hundred nanograms of total RNA was retrotranscribed using the Superscript III kit (Invitrogen) following the manufacturer's instructions. The cDNAs obtained after the retrotranscription were used as templates for quantitative PCR as described^(43,64). The reaction was performed with a Roche480 thermal cycler using the Absolute Blue QPCR SYBR Green Mix from Thermo Scientific. The relative amount of specific mRNA was normalized to GAPDH. Results are presented as the mean±s.d. of triplicate amplifications. The validation of fusion transcripts was performed using both genomic PCR and RT-PCR with forward and reverse primer combinations designed within the margins of the paired-end read sequences detected by RNA-seq. Expressed fusion transcript variants were subjected to direct sequencing to confirm the sequence and translation frame. The primers used for the screening of gene fusions are detailed in Table 17. The primers used for genomic detection of gene fusions are listed in Table 18. Semiquantitative RT-PCR to detect exogenous wild-type MYC-LZTR1 and mutant p.Arg801Trp LZTR1 was performed using the primers listed in Table 19.

Subcutaneous Xenografts and Drug Treatment.

Female athymic mice (nu/nu genotype, BALB/c background, 6-8 weeks old) were used for all antitumor studies. Patient-derived adult human glioblastoma xenografts were maintained. Xenografts were excised from host mice under sterile conditions and homogenized with the use of a tissue press and modified tissue cytosieve (Biowhitter Inc.), and tumor homogenate was loaded into a repeating Hamilton syringe (Hamilton, Co.) dispenser. Cells were injected subcutaneously into the right flank of the athymic mouse at an inoculation volume of 50 ml with a 19-gauge needle⁶⁵.

Subcutaneous tumors were measured twice weekly with hand-held vernier calipers (Scientific Products). Tumor volumes (V) were calculated with the following formula: ((width)×(length))/2=V (mm³) For the subcutaneous tumor studies, groups of mice randomly selected by tumor volume were treated with EGFR kinase inhibitors when the median tumor volumes were an average of 150 mm³ and were compared with control animals receiving vehicle (saline).

Erlotinib was administered at 100 mg per kg body weight orally once per day for 10 d. Lapatinib was administered at 75 mg per kg body weight orally twice per day for 20 d. Response to treatment was assessed by a delay in tumor growth and tumor regression.

Growth delay, expressed as a T-C value, is defined as the difference in days between the median time required for tumors in treated and control animals to reach a volume five times greater than that measured at the start of the treatment. Tumor regression is defined as a decrease in tumor volume over two successive measurements. Statistical analysis was performed using a SAS statistical analysis program, the Wilcoxon rank-order test for growth delay and Fisher's exact test for tumor regression.

Intracranial Injection.

GBM-derived primary cells were first infected with a lentivirus expressing luciferase and subsequently transduced with the pLOC vector or pLOC-CTNND2 lentiviral particles. Intracranial injection was performed in 9-week-old male nu/nu mice (Charles River Laboratories). Briefly, 5≦10⁵ cells were resuspended in 2.5 μl of PBS and injected into the caudate putamen using a stereotaxic frame (coordinates relative to the bregma: 0.6 mm anterior; 1.65 mm medium-lateral; 3 mm depth-ventral). Tumor growth was monitored using the IVIS Imaging system. Briefly, mice were anesthetized with 3% isoflurane before intraperitoneal injection of 100 mg per kg body weight n-luciferin (Xenogen). Ten minutes after injection of n-luciferin, images were acquired for 1 min with the Xenogen IVIS system (Xenogen) using Living Image acquisition and analysis software (Xenogen). The bioluminescent signal was expressed in photons per second and displayed as a pseudo-color image representing the spatial distribution of photon counts.

URLs.

DNA and RNA sequencing and copy number variant data in The Cancer Genome Atlas (TCGA), http://cancergenome.nih.gov; glioma patient survival data from the Repository for Molecular Brain Neoplasia Data (REMBRANDT), https://caintegrator.nci.nih.gov/rembrandt/; sequence data deposition in database of Genotypes and Phenotypes (dbGaP), http://www.ncbi.nlm.nih.gov/gap; gene fusion annotation software package Pegasus, http://sourceforge.net/projects/pegasus-fus/.

Data Access.

RNA sequencing of twenty-four human GBM sphere cultures in this study were deposited under the dbGaP study accession phs000505.v2.p1. RNA and DNA sequencing of TCGA GBM samples was also analyzed from the dbGaP study accession phs000178.v1.p1.

REFERENCES FOR EXAMPLE 2

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Tables and Legends for Examples

TABLE 7 Gene fusions identified through RNA sequencing. Table 7. Gene fusions identified through RNA sequencing. sample #chrom 5p start5p end5p Chrom 3p Start 3p End 3p G17807.TCGA-28-5209- chr7 55086724 55268105 chr7 56078745 56079561 01A-01R-1850-01.4 G17197.TCGA-06-0211- chr7 55433140 55479781 chr7 55861236 55886915 01B-01R-1849-01.2 G17650.TCGA-28-2513- chr7 55086724 55268105 chr7 55861236 55863784 01A-01R-1850-01.2 G17506.TCGA-27-1835- chr4 1795038 1808660 chr4 1741428 1746894 01A-01R-1850-01.2 G17191.TCGA-06-0211- chr7 55433140 55479781 chr7 55861236 55886915 01A-01R-1849-01.2 G17512.TCGA-27-1837- chr7 55086724 55268105 chr7 55861236 55863784 01A-01R-1850-01.2 NYU_A chr4 1795038 1808660 chr4 1737457 1746894 G17814.TCGA-06-5411- chr1 204797781 204951147 chr1 156844362 156851641 01A-01R-1849-01.4 G17223.TCGA-06-0750- chr7 55177539 55268105 chr7 55861236 55863784 01A-01R-1849-01.2 G17798.TCGA-32-5222- chr7 55086724 55268105 chr7 55861236 55863784 01A-01R-1850-01.4 G17195.TCGA-06-0138- chr12 69753531 69764754 chr12 58339410 58351050 01A-02R-1849-01.2 G17803.TCGA-76-4925- chr4 1795038 1808660 chr4 1739324 1746894 01A-01R-1850-01.4 NYU_B chr17 7387849 7388175 chr17 7604058 7605804 G17507.TCGA-28-1747- chr7 55086724 55268105 chr7 55861236 55863784 01C-01R-1850-01.2 G17469.TCGA-06-2557- chr7 7388705 73604247 chr7 74173109 74175019 01A-01R-1849-01.2 G17785.TCGA-06-5413- chr14 32798478 32903022 chr14 34393422 34400420 01A-01R-1849-01.4 G17467.TCGA-14-0736- chr14 102606211 102606508 chr19 12856190 12859137 02A-01R-2005-01.2 GBM-CUMC3316_L1 chr22 22160138 22221969 chr12 58166799 58176322 G17663.TCGA-19-2619- chr1 156611739 156628524 chr1 156844697 156851641 01A-01R-1850-01.2 G17203.TCGA-06-0211- chr7 54825187 54826938 chr7 55224225 55224641 02A-02R-2005-01.2 G17784.TCGA-76-4929- chr2 9675962 9695916 chr2 9724106 9731643 01A-01R-1850-01.4 G17675.TCGA-19-2624- chr7 55086724 55240816 chr12 65107223 65110598 01A-01R-1850-01.2 G17796.TCGA-41-5651- chr12 58166382 58166910 chr12 58162351 58163738 01A-01R-1850-01.4 G17666.TCGA-06-5415- chr5 134209459 134210219 chr2 219103386 219119069 01A-01R-1849-01.2 G17219.TCGA-06-0158- chr2 42396489 42396775 chrX 41374190 41420896 01A-01R-1849-01.2 G17790.TCGA-06-5856- chr12 122150657 122150869 chr12 58191442 58193702 01A-01R-1849-01.4 NYU_B chr1 19746154 19811991 chr1 19401001 19433459 G17657.TCGA-19-1787- chr3 100428159 100438901 chr3 100348441 100414320 01B-01R-1850-01.2 G17643.TCGA-12-5295- chr20 43976964 43977063 chr3 52740659 52742194 01A-01R-1849-01.2 NYU_G chr5 100191806 100238986 chr5 102260660 102365415 G17494.TCGA-14-2554- chr3 48956280 48965245 chr3 48265643 48266974 01A-01R-1850-01.2 G17196.TCGA-06-0178- chr12 58123421 58135939 chr8 94827532 94830345 01A-01R-1849-01.2 G17782.TCGA-26-5136- chr1 95392393 95392734 chr1 95448278 95448861 01B-01R-1850-01.4 GBM-CUMC3296_L1 chr7 55639963 55640199 chr12 68642024 68645357 G17199.TCGA-06-0744- chr7 55086724 55087057 chr9 102741464 102784507 01A-01R-1849-01.2 G17792.TCGA-28-5204- chr4 6988888 6996028 chr4 8288287 8298197 01A-01R-1850-01.4 G17476.TCGA-06-2569- chr6 7310149 7313540 chrX 31137344 32328392 01A-01R-1849-01.2 G17195.TCGA-06-0138- chr12 69139935 69145969 chr12 58109542 58115337 01A-02R-1849-01.2 G17212.TCGA-06-0129- chr5 140855568 140858112 chr6 163956013 163991168 01A-01R-1849-01.2 G17213.TCGA-06-0157- chr4 2061586 2062888 chr16 90071278 90075837 01A-01R-1849-01.2 G17200.TCGA-06-0125- chr1 27022521 27094489 chr14 24624395 24630546 01A-01R-1849-01.2 G17804.TCGA-06-5408- chr7 55086724 55268105 chr7 56078745 56079561 01A-01R-1849-01.4 G17656.TCGA-28-2514- chr1 27022521 27024030 chr1 49493541 49202173 01A-02R-1850-01.2 G17654.TCGA-41-4097- chr5 146017813 146461053 chr1 156278751 156294879 01A-01R-1850-01.2 G17206.TCGA-06-0125- chr1 27022521 27094489 chr14 24624365 24630546 02A-11R-2005-01.2 G17792.TCGA-28-5204- chr9 36190891 36204175 chr9 33911961 33920398 01A-01R-1850-01.4 G17663.TCGA-19-2619- chr1 205719084 205719360 chr1 205797153 205811016 01A-01R-1850-01.2 NYU_E chr16 69221049 69333676 chr16 69349910 69358944 NYU_G chr19 42759129 42759308 chr19 42734337 42744293 NYU B chr12 6457892 6473312 chr12 6437923 6443409 G17675.TCGA-19-2624- chr12 69201970 69230528 chr12 63037762 63195939 01A-01R-1850-01.2 G17484.TCGA-14-0787- chr1 155385534 155532323 chr1 156374054 156384544 01A-01R-1849-01.2 G17792.TCGA-28-5204- chr7 100065174 100076901 chr7 100054237 100061308 01A-01R-1850-01.4 BT299 chr1 23037330 23037535 chr1 1246964 1256472 G17667.TCGA-26-5134- chr4 54373483 54424435 chr4 53457128 53494329 01A-01R-1850-01.2 GBM-CUMC3338_L1 chr19 41198855 41207363 chr19 41171813 41192899 G17815.TCGA-19-5960- chr1 154918047 154928566 chr1 154897208 154904890 01A-11R-1850-01.4 G17662.TCGA-32-1970- chr19 58740069 58758159 chr19 50285013 50310366 01A-01R-1850-01.2 NYU_E chr7 65540775 65557649 chr7 65592690 54519550 G17816.TCGA-28-5215- chr7 55086724 55268105 chr7 56078745 56079561 01A-01R-1850-01.4 G17650.TCGA-28-2513- chr7 55433140 55433921 chr7 55861236 55914329 01A-01R-1850-01.2 BT308 chr20 33222418 33265088 chr20 33302578 33303168 G17656.TCGA-28-2514- chr7 55086724 55268105 chr7 55538305 55588822 01A-02R-1850-01.2 G17639.TCGA-12-3652- chr9 33290509 33295424 chr9 34379016 34382866 01A-01R-1849-01.2 G17796.TCGA-41-5651- chr12 58087885 58090155 chr12 57960908 57978553 01A-01R-1850-01.4 G17468.TCGA-19-0957- chr1 61547979 61554351 chr10 90043860 90122481 02A-11R-2005-01.2 G17790.TCGA-06-5856- chr13 20304378 20357082 chr13 20977808 20987525 01A-01R-1849-01.4 GBM-CUMC3338_L1 chr17 7465318 7470321 chr17 7215977 7217039 G17790.TCGA-06-5856- chr12 117175594 117175842 chr12 69229608 69239210 01A-01R-1849-01.4 G17802.TCGA-28-5208- chr7 51203854 51258774 chr7 55861236 55886915 01A-01R-1850-01.4 G17210.TCGA-12-0616- chr7 101006121 101176423 chr7 30536238 30536850 01A-01R-1849-01.2 NYU_B chr2 233562014 233613791 chr2 234867560 234928164 G17469.TCGA-06-2557- chr7 55086724 55268105 chr7 55861236 55863784 01A-01R-1849-01.2 G17480.TCGA-27-1830- chr2 2319216080 231945027 chr2 230222345 230377651 01A-01R-1850-01.2 G17634.TCGA-19-2625- chr22 36424287 36424584 chr22 37966253 37967937 01A-01R-1850-01.2 G17654.TCGA-41-4097- chr3 66119284 66313802 chr2 86371055 86374955 01A-01R-1850-01.2 G17485.TCGA-14-1402- chr3 142166711 142166852 chr1 245912644 246093238 02A-01R-2005-01.2 G17498.TCGA-02-2483- chr9 119976636 120177316 chr16 332024 333367 01A-01R-1849-01.2 G17799.TCGA-06-1804- chr13 60971426 61109366 chr13 47345391 47345630 01A-01R-1849-01.4 G17660.TCGA-06-5414- chr8 61591338 61655655 chr8 59717976 59872566 01A-01R-1849-01.2 GBM-CUMC3296_L1 chr12 67663060 69688935 chr7 55238867 55275029 G17505.TCGA-06-2564- chr5 216843 218296 chr5 1253286 1282738 01A-01R-1849-01.2 G17798.TCGA-32-5222- chr1 11313895 11322607 chr1 6880240 6932096 01A-01R-1850-01.4 GBM-CUMC3297_L1 chr22 24640520 24641109 chr22 18659538 18660159 GBM-CUMC3342_L1 chr10 61083747 61122351 chr10 104375024 104378415 G17500.TCGA-27-1831- chr13 39261172 39438742 chr13 41790516 41808142 01A-01R-1850-01.2 G17212.TCGA-06-0129- chr6 3410421 3456792 chr6 47199268 47221256 01A-01R-1849-01.2 GBM-CUMC3322_L1 chr7 141251077 141255366 chr7 158715067 158738881 G17675.TCGA-19-2624- chr12 54378945 54379793 chr12 56295196 56297263 01A-01R-1850-01.2 G17803.TCGA-76-4925- chr17 74046508 74068577 chr19 10683347 10694745 01A-01R-1850-01.4 G17796.TCGA-41-5651- chr12 58176535 58186855 chr12 57849876 57851788 01A-01R-1850-01.4 G17663.TCGA-19-2619- chr7 70597788 70800718 chr7 94827660 94925724 01A-01R-1850-01.2 G17207.TCGA-06-0156- chr11 910774 910873 chr16 4390252 4438631 01A-03R-1849-01.2 G17802.TCGA-28-5208- chr7 55433140 55433921 chr7 56078745 56079561 01A-01R-1850-01.4 G17485.TCGA-14-1402- chr7 151216545 151217009 chr7 151253202 151372722 02A-01R-2005-01.2 NYU_E chr11 88033697 88070940 chr11 87846430 87883122 G17212.TCGA-06-0129- chr12 51079615 51128912 chr6 42029094 42048642 01A-01R-1849-01.2 G17787.TCGA-26-5139- chr19 13915605 13920033 chr1 156005092 156012703 01A-01R-1850-01.4 G17675.TCGA-19-2624- chr12 65218409 65232630 chr12 63037762 63226038 01A-01R-1850-01.2 G17800.TCGA-06-5859- chr18 48556582 48586285 chr18 56934268 56936732 01A-01R-1849-01.4 G17638.TCGA-28-2499- chr2 234263152 234299128 chr2 234967479 234978666 01A-01R-1850-01.2 Total frags Spanning Strand (split inserts + frags (split sample 5p Strand 3p Genes 5p Genes 3p split reads) reads) G17807.TCGA-28-5209- + − EGFR PSPH 6849 5648 01A-01R-1850-01.4 G17197.TCGA-06-0211- + − LANCL2 SEPT14 2619 2078 01B-01R-1849-01.2 G17650.TCGA-28-2513- + − EGFR SEPT14 1899 1464 01A-01R-1850-01.2 G17506.TCGA-27-1835- + + FGFR3 TACC3 1749 1604 01A-01R-1850-01.2 G17191.TCGA-06-0211- + − LANCL2 SEPT14 1367 1128 01A-01R-1849-01.2 G17512.TCGA-27-1837- + − EGFR SEPT14 989 796 01A-01R-1850-01.2 NYU_A + + FGFR3 TACC3 973 492 G17814.TCGA-06-5411- + + KIAA0756, NTRK1 841 751 01A-01R-1849-01.4 NFASC G17223.TCGA-06-0750- + − EGFR SEPT14 534 414 01A-01R-1849-01.2 G17798.TCGA-32-5222- + − EGFR SEPT14 528 495 01A-01R-1850-01.4 G17195.TCGA-06-0138- + + YEATS4 XRCC6BP1 328 306 01A-02R-1849-01.2 G17803.TCGA-76-4925- + + FGFR3 TACC3 303 203 01A-01R-1850-01.4 NYU_B + + POLR2A WRAP53 263 240 G17507.TCGA-28-1747- + − EGFR SEPT14 181 142 01C-01R-1850-01.2 G17469.TCGA-06-2557- + + EIF4H GTF2I 180 142 01A-01R-1849-01.2 G17785.TCGA-06-5413- + − AKAP6 EGLN3 171 129 01A-01R-1849-01.4 G17467.TCGA-14-0736- + + WDR20 ASNA1 151 75 02A-01R-2005-01.2 GBM-CUMC3316_L1 − + MAPK1 FAM119B, 145 96 DKFZp586D0919 G17663.TCGA-19-2619- + + BCAN NTRK1 130 17 01A-01R-1850-01.2 G17203.TCGA-06-0211- − + SEC61G EGFR 129 103 02A-02R-2005-01.2 G17784.TCGA-76-4929- − − ADAM17 YWHAQ 106 95 01A-01R-1850-01.4 G17675.TCGA-19-2624- + − EGFR GNS 92 59 01A-01R-1850-01.2 G17796.TCGA-41-5651- + − FAM1198, METTL1 29 18 01A-01R-1850-01.4 DKFZp586D0919 G17666.TCGA-06-5415- + + TXNDC15 ARPC2 90 36 01A-01R-1849-01.2 G17219.TCGA-06-0158- + − EML4 CASK 86 63 01A-01R-1849-01.2 G17790.TCGA-06-5856- + − TMEM120B AVIL 75 56 01A-01R-1849-01.4 NYU_B − − CAPZB UBR4 72 48 G17657.TCGA-19-1787- + + TFG GPR128 23 19 01B-01R-1850-01.2 G17643.TCGA-12-5295- − + SDC4 SPCS1 68 18 01A-01R-1849-01.2 NYU_G − + ST8SIA4 PAM 60 55 G17494.TCGA-14-2554- + + Arl2, ARIH2 CAMP 59 52 01A-01R-1850-01.2 G17196.TCGA-06-0178- − + AGAP2 TMEM67 59 21 01A-01R-1849-01.2 G17782.TCGA-26-5136- − − CNN3 ALG14 54 49 01B-01R-1850-01.4 GBM-CUMC3296_L1 − − VOPP1 IL22 48 35 G17199.TCGA-06-0744- + − EGFR ERP44, 46 30 01A-01R-1849-01.2 KIAA0573 G17792.TCGA-28-5204- + + TBC1D14 HTRA3 45 33 01A-01R-1850-01.4 G17476.TCGA-06-2569- − − SSR1 DM0 44 33 01A-01R-1849-01.2 G17195.TCGA-06-0138- + + SLC35E3 O59 44 38 01A-02R-1849-01.2 G17212.1CGA-06-0129- + + PCDHGC3, QKI 43 24 01A-01R-1849-01.2 PCDHGC4 G17213.TCGA-06-0157- + − NAT8L DBNDD1, 39 24 01A-01R-1849-01.2 DKFZp761L2416 G17200.TCGA-06-0125- + + ARID1A hoip, RNF31 39 26 01A-01R-1849-01.2 G17804.TCGA-06-5408- + − EGFR PSPH 38 37 01A-01R-1849-01.4 G17656.TCGA-28-2514- + − ARID1A BEND5 37 29 01A-02R-1850-01.2 G17654.TCGA-41-4097- − − PPP2R2B CCT3, 37 18 01A-01R-1850-01.2 DKFZp667A196 G17206.TCGA-06-0125- + + ARID1A hoip, RNF31 36 21 02A-11R-2005-01.2 G17792.TCGA-28-5204- + + CLTA UBE2R2 36 31 01A-01R-1850-01.4 G17663.TCGA-19-2619- − − NUCKS1 PM20D1 34 31 01A-01R-1850-01.2 NYU_E + + SNTB2 VPS4A 14 13 NYU_G − − ERF GSK3A 14 3 NYU_B − − SCNN1A TNFRSF1A 13 9 G17675.TCGA-19-2624- + − MDM2 PPM1H 34 22 01A-01R-1850-01.2 G17484.TCGA-14-0787- − − ASH1L C1orf61 33 30 01A-01R-1849-01.2 G17792.TCGA-28-5204- − − TSC22D4 C7orf61 12 1 01A-01R-1850-01.4 BT299 + − EPHB2 CPSF3L 33 6 G17667.TCGA-26-5134- − − LNX1 USP46 33 27 01A-01R-1850-01.2 GBM-CUMC3338_L1 − − ADCK4 NUMBL 11 4 G17815.TCGA-19-5960- − − PBXIP1 PMVK 10 8 01A-11 R-1850-01.4 G17662.TCGA-32-1970- + + ZNF544 DKFZp586H1320, 31 28 01A-01R-1850-01.2 AP2A1 NYU_E + + ASL CRCP 10 8 G17816.TCGA-28-5215- + − EGFR PSPH 31 28 01A-01R-1850-01.4 G17650.TCGA-28-2513- + − LANCL2 SEPT14 31 14 01A-01R-1850-01.2 BT308 − − PIGU NCOA6 30 26 G17656.TCGA-28-2514- + − EGFR GASP, 01A-02R-1850-01.2 VOPP1 29 23 G17639.TCGA-12-3652- + − NFX1 C9orf24 28 20 01A-01R-1849-01.2 G17796.TCGA-41-5651- + + OS9 KIF5A 28 23 01A-01R-1850-01.4 G17468.1CGA-19-0957- + − NFIA RNLS,  27 14 02A-11R-2005-01.2 C1orf59 G17790.TCGA-06-5856- − − PSPC1 CRYL1 26 18 01A-01R-1849-01.4 GBM-CUMC3338_L1 + − SENP3 GPS2, 26 15 KIAA1787 G17790.TCGA-06-5856- − + C12orf49 MDM2 26 16 01A-01R-1849-01.4E G17802.TCGA-28-5208- − − COBL SEPT14 23 15 01A-01R-1850-01.4 G17210.TCGA-12-0616- + − EMID2 GGCT 22 16 01A-01R-1849-01.2 NYU_B + + KIAA0642, TRPMB 22 20 GIGYF2 G17469.TCGA-06-2557- + − EGFR SEPT14 21 13 01A-01R-1849-01.2 G17480.TCGA-27-1830- + − PSMD1 DNER 20 14 01A-01R-1850-01.2 G17634.TCGA-19-2625- − − RBM9 LGALS2 20 16 01A-01R-1850-01.2 G17654.TCGA-41-4097- + − SLC25A26 IMMT 19 17 01A-01R-1850-01.2 G17485.TCGA-14-1402- − − XRN1 SMYD3 19 11 02A-01R-2005-01.2 G17498.TCGA-02-2483- − + ASTN2 ARHGDIG, 18 6 01A-01R-1849-01.2 PDIA2 G17799.TCGA-06-1804- + − TDRD3 ESD 18 13 01A-01R-1849-01.4 G17660.TCGA-06-5414- + − CHD7 TOX 18 16 01A-01R-1849-01.2 GBM-CUMC3296_L1 + + CAND1 EGFR 17 14 G17505.TCGA-06-2564 − − CCDC127 hTERT, TERT 17 12 01A-01R-1849-01.2 G17798.TCGA-32-5222- − + MTOR KIAA0833, 17 13 01A-01R-1850-01.4 CAMTA1 GBM-CUMC3297_L1 − + DKFZp566O011, USP18 16 6 GGT5 GBM-CUMC3342_L1 − + FAM13C DKFZp434E2022, 15 11 SUFU G17500.TCGA-27-1831- + − FREM2 MTRF1 15 14 01A-01R-1850-01.2 G17212.TCGA-06-0129- − − SLC22A23, TNFRSF21 15 11 01A-01R-1849-01.2 DKFZp434F011 GBM-CUMC3322_L1 + + AGK WDR60 15 12 G17675.TCGA-19-2624- + − HOXC10 WIBG 15 10 01A-01R-1850-01.2 G17803.TCGA-76-4925- − − SRP68 AP1M2 14 8 01A-01R-1850-01.4 G17796.TCGA-41-5651- + + TSFM INHBE 14 9 01A-01R-1850-01.4 G17663.TCGA-19-2619- + + WBSCR17 PPP1R9A 14 10 01A-01R-1850-01.2 G17207.TCGA-06-0156- − − CHID1 Magmas, hCG_ 13 13 01A-03R-1849-01.2 1787779, CORO7 G17802.TCGA-28-5208- + − LANCL2 PSPH 13 2 01A-01R-1850-01.4 G17485.TCGA-14-1402- − − RHEB H91620, 12 11 02A-01R-2005-01.2 PRKAG2 NYU_E − − CTSC RAB38 12 11 G17212.TCGA-06-0129- + + DIP2B TAF8 12 7 01A-01R-1849-01.2 G17787.TCGA-26-5139- + − ZSW1M4 UBQLN4 11 9 01A-01R-1850-01.4 G17675.TCGA-19-2624- + − TBC1030, PPM1H 10 6 01A-01R-1850-01.2 KIAA0984 G17800.TCGA-06-5859- + − SMAD4 RAX 10 10 01A-01R-1849-01.4 G17638.TCGA-28-2499- + + DGKD SPP2 10 10 01A-01R-1850-01.2 Gene Break- Gene Break- Frame SEQ ID sample point 5p point 3p Type NO Fused Sequence G17807. 56268106 56079562 InFrame 8276 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-28- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 5209- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01A-01R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1850- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.4 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAGTGATGCT TTCATTGGATTTGGAGGAAATGTGATCAGGCAACAAG TCAAGGATAACGCCAAATGGTATATCACTGATTTTGTA GAGCTGCTGGGAGAACTGGAAGAA G17197. 55479782 55886916 InFrame 8277 ATGGGCGAGACCATGTCAAAGAGGCTGAAGCTCCACC TCGA-06- TGGGAGGGGAGGCAGAAATGGAGGAACGGGCGTTCG 0211- TCAACCCCTTCCCGGACTACGAGGCCGCCGCCGGGGC 01G-01R- GCTGCTCGCCTCCGGAGCGGCCGAAGAGACAGGCTGT 1849- GTTCGTCCCCCGGCGACCACGGATGAGCCCGGCCTCCC 01.2 TTTTCATCAGGACGGGAAGATCATTCATAATTTCATAA GACGGATCCAGACCAAAATTAAAGATCTTCTGCAGCA AATGGAAGAAGGGCTGAAGACAGCTGATCCCCATGAC TGCTCTGCTTATACTGGCTGGACAGGCATAGCCCTTTT GTACCTGCAGTTGTACCGGGTCACATGTGACCAAACCT ACCTGCTCCGATCCCTGGATTACGTAAAAAGAACACTT CGGAATCTGAATGGCCGCAGGGTCACCTTCCTCTGTGG GGATGCTGGCCCCCTGGCTGTTGGAGCTGTGATTTATC ACAAACTCAGAAGTGACTGTGAGTCCCAGGAATGTGT CACAAAACTTTTGCAGCTCCAGAGATCGGTTGTCTGCC AAGAATCAGACCTTCCTGATGAGCTGCTTTATGGACGG GCAGGTTATCTGTATGCCTTACTGTACCTGAACACAGA GATAGGTCCAGGCACCGTGTGTGAGTCAGCTATTAAA GAGGTAGTCAATGCTATTATTGAATCGGGTAAGACTTT GTCAAGGGAAGAAAGAAAAACGGAGCGCTGCCCGCT GTTGTACCAGTGGCACCGGAAGCAGTACGTTGGAGCA GCCCATGGCATGGCTGGAATTTACTATATGTTAATGCA GCCGGCAGCAAAAGTGGACCAAGAAACCTTGACAGAA ATGGTGAAACCCAGTATTGATTATGTGCGCCACAAAAA ATTCCGATCTGGGAATTACCCATCATCATTAAGCAATG AAACAGACCGGCTGGTGCACTGGTGCCACGGCGCCCC GGGGGTCATCCACATGCTCATGCAGGCGTACAAG|GG GCTGTTACCCTTTGCTGTGGTAGGGAGTACAGATGAA GTGAAAGTTGGAAAAAGGATGGTCAGAGGCCGTCACT ACCCTTGGGGAGTTTTGCAAGTGGAAAATGAAAATCA CTGTGACTTCGTTAAGCTCCGAGATATGCTTCTTTGTAC CAATATGGAAAATCTAAAAGAAAAAACCCACACTCAG CACTATGAATGTTATAGGTACCAAAAACTGCAGAAAAT GGGCTTTACAGATGTGGGTCCAAACAACCAGCCAGTT AGTTTTCAAGAAATCTTTGAAGCCAAAAGACAAGAGTT CTATGATCAATGTCAGAGGGAAGAAGAAGAGTTGAAA CAGAGATTTATGCAGCGAGTCAAGGAGAAAGAAGCAA CATTTAAAGAAGCTGAAAAAGAGCTGCAGGACAAGTT CGAGCATCTTAAAATGATTCAACAGGAGGAGATAAGG AAGCTCGAGGAAGAGAAAAAACAACTGGAAGGAGAA ATCATAGATTTTTATAAAATGAAAGCTGCCTCCGAAGC ACTGCAGACTCAGCTGAGCACCGATACAAAGAAAGAC AAACATCGTAAGAAA G17650. 55268106 55863785 InFrame 8278 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-28- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 2513- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01A-01R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1850- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.2 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAG|CTGCAG GACAAGTTCGAGCATCTTAAAATGATTCAACAGGAGG AGATAAGGAAGCTCGAGGAAGAGAAAAAACAACTGG AAGGAGAAATCATAGATTTTTATAAAATGAAAGCTGCC TCCGAAGCACTGCAGACTCAGCTGAGCACCGATACAA AGAAAGACAAACATCGTAAGAAA G17506. 1808661 1741429 InFrame 8279 ATGGGCGCCCCTGCCTGCGCCCTCGCGCTCTGCGTGGC TCGA-27- CGTGGCCATCGTGGCCGGCGCCTCCTCGGAGTCCTTG 1835- GGGACGGAGCAGCGCGTCGTGGGGCGAGCGGCAGAA 01A-01R- GTCCCGGGCCCAGAGCCCGGCCAGCAGGAGCAGTTG 1850- GTCTTCGGCAGCGGGGATGCTGTGGAGCTGAGCTGTC 01.2 CCCCGCCCGGGGGTGGTCCCATGGGGCCCACTGTCTG GGTCAAGGATGGCACAGGGCTGGTGCCCTCGGAGCGT GTCCTGGTGGGGCCCCAGCGGCTGCAGGTGCTGAATG CCTCCCACGAGGACTCCGGGGCCTACAGCTGCCGGCA GCGGCTCACGCAGCGCGTACTGTGCCACTTCAGTGTGC GGGTGACAGACGCTCCATCCTCGGGAGATGACGAAGA CGGGGAGGACGAGGCTGAGGACACAGGTGTGGACAC AGGGGCCCCTTACTGGACACGGCCCGAGCGGATGGAC AAGAAGCTGCTGGCCGTGCCGGCCGCCAACACCGTCC GCTTCCGCTGCCCAGCCGCTGGCAACCCCACTCCCTCC ATCTCCTGGCTGAAGAACGGCAGGGAGTTCCGCGGCG AGCACCGCATTGGAGGCATCAAGCTGCGGCATCAGCA GTGGAGCCTGGTCATGGAAAGCGTGGTGCCCTCGGAC CGCGGCAACTACACCTGCGTCGTGGAGAACAAGTTTG GCAGCATCCGGCAGACGTACACGCTGGACGTGCTGGA GCGCTCCCCGCACCGGCCCATCCTGCAGGCGGGGCTG CCGGCCAACCAGACGGCGGTGCTGGGCAGCGACGTG GAGTTCCACTGCAAGGTGTACAGTGACGCACAGCCCC ACATCCAGTGGCTCAAGCACGTGGAGGTGAATGGCAG CAAGGTGGGCCCGGACGGCACACCCTACGTTACCGTG CTCAAGTCCTGGATCAGTGAGAGTGTGGAGGCCGACG TGCGCCTCCGCCTGGCCAATGTGTCGGAGCGGGACGG GGGCGAGTACCTCTGTCGAGCCACCAATTTCATAGGC GTGGCCGAGAAGGCCTTTTGGCTGAGCGTTCACGGGC CCCGAGCAGCCGAGGAGGAGCTGGTGGAGGCTGACG AGGCGGGCAGTGTGTATGCAGGCATCCTCAGCTACGG GGTGGGCTTCTTCCTGTTCATCCTGGTGGTGGCGGCTG TGACGCTCTGCCGCCTGCGCAGCCCCCCCAAGAAAGG CCTGGGCTCCCCCACCGTGCACAAGATCTCCCGCTTCC CGCTCAAGCGACAGGTGTCCCTGGAGTCCAACGCGTC CATGAGCTCCAACACACCACTGGTGCGCATCGCAAGG CTGTCCTCAGGGGAGGGCCCCACGCTGGCCAATGTCT CCGAGCTCGAGCTGCCTGCCGACCCCAAATGGGAGCT GTCTCGGGCCCGGCTGACCCTGGGCAAGCCCCTTGGG GAGGGCTGCTTCGGCCAGGTGGTCATGGCGGAGGCC ATCGGCATTGACAAGGACCGGGCCGCCAAGCCTGTCA CCGTAGCCGTGAAGATGCTGAAAGACGATGCCACTGA CAAGGACCTGTCGGACCTGGTGTCTGAGATGGAGATG ATGAAGATGATCGGGAAACACAAAAACATCATCAACC TGCTGGGCGCCTGCACGCAGGGCGGGCCCCTGTACGT GCTGGTGGAGTACGCGGCCAAGGGTAACCTGCGGGA GTTTCTgcgggcgcggcggcccccgggccTGGACTACTCCTTC GACACCTGCAAGCCGCCCGAGGAGCAGCTCACCTTCA AGGACCTGGTGTCCTGTGCCTACCAGGTGGCCCGGGG CATGGAGTACTTGGCCTCCCAGAAGTGCATCCACAGG GACCTGGCTGCCCGCAATGTGCTGGTGACCGAGGACA ACGTGATGAAGATCGCAGACTTCGGGCTGGCCCGGGA CGTGCACAACCTCGACTACTACAAGAAGACGACCAAC GGCCGGCTGCCCGTGAAGTGGATGGCGCCTGAGGCCT TGTTTGACCGAGTCTACACTCACCAGAGTGACGTCTGG TCCTTTGGGGTCCTGCTCTGGGAGATCTTCACGCTGGG GGGCTCCCCGTACCCCGGCATCCCTGTGGAGGAGCTCT TCAAGCTGCTGAAGGAGGGCCACCGCATGGACAAGCC CGCCAACTGCACACACGACCTGTACATGATCATGCGG GAGTGCTGGCATGCCGCGCCCTCCCAGAGGCCCACCTT CAAGCAGCTGGTGGAGGACCTGGACCGTGTCCTTACC GTGACGTCCACCGAC|GTAAAGGCGACACAGGAGGAG AACCGGGAGCTGAGGAGCAGGTGTGAGGAGCTCCAC GGGAAGAACCTGGAACTGGGGAAGATCATGGACAGG TTCGAAGAGGTTGTGTACCAGGCCATGGAGGAAGTTC AGAAGCAGAAGGAACTTTCCAAAGCTGAAATCCAGAA AGTTCTAAAAGAAAAAGACCAACTTACCACAGATCTGA ACTCCATGGAGAAGTCCTTCTCCGACCTCTTCAAGCGT TTTGAGAAACAGAAAGAGGTGATCGAGGGCTACCGCA AGAACGAAGAGTCACTGAAGAAGTGCGTGGAGGATT ACCTGGCAAGGATCACCCAGGAGGGCCAGAGGTACCA AGCCCTGAAGGCCCACGCGGAGGAGAAGCTGCAGCT GGCAAACGAGGAGATCGCCCAGGTCCGGAGCAAGGC CCAGGCGGAAGCGTTGGCCCTCCAGGCCAGCCTGAGG AAGGAGCAGATGCGCATCCAGTCGCTGGAGAAGACA GTGGAGCAGAAGACTAAAGAGAACGAGGAGCTGACC AGGATCTGCGACGACCTCATCTCCAAGATGGAGAAGA TC G17191. 55479782 55886916 InFrame 8280 ATGGGCGAGACCATGTCAAAGAGGCTGAAGCTCCACC TCGA-06- TGGGAGGGGAGGCAGAAATGGAGGAACGGGCGTTCG 0211- TCAACCCCTTCCCGGACTACGAGGCCGCCGCCGGGGC 01A-01R- GCTGCTCGCCTCCGGAGCGGCCGAAGAGACAGGCTGT 1849- GTTCGTCCCCCGGCGACCACGGATGAGCCCGGCCTCCC 01.2 TTTTCATCAGGACGGGAAGATCATTCATAATTTCATAA GACGGATCCAGACCAAAATTAAAGATCTTCTGCAGCA AATGGAAGAAGGGCTGAAGACAGCTGATCCCCATGAC TGCTCTGCTTATACTGGCTGGACAGGCATAGCCCTTTT GTACCTGCAGTTGTACCGGGTCACATGTGACCAAACCT ACCTGCTCCGATCCCTGGATTACGTAAAAAGAACACTT CGGAATCTGAATGGCCGCAGGGTCACCTTCCTCTGTGG GGATGCTGGCCCCCTGGCTGTTGGAGCTGTGATTTATC ACAAACTCAGAAGTGACTGTGAGTCCCAGGAATGTGT CACAAAACTTTTGCAGCTCCAGAGATCGGTTGTCTGCC AAGAATCAGACCTTCCTGATGAGCTGCTTTATGGACGG GCAGGTTATCTGTATGCCTTACTGTACCTGAACACAGA GATAGGTCCAGGCACCGTGTGTGAGTCAGCTATTAAA GAGGTAGTCAATGCTATTATTGAATCGGGTAAGACTTT GTCAAGGGAAGAAAGAAAAACGGAGCGCTGCCCGCT GTTGTACCAGTGGCACCGGAAGCAGTACGTTGGAGCA GCCCATGGCATGGCTGGAATTTACTATATGTTAATGCA GCCGGCAGCAAAAGTGGACCAAGAAACCTTGACAGAA ATGGTGAAACCCAGTATTGATTATGTGCGCCACAAAAA ATTCCGATCTGGGAATTACCCATCATCATTAAGCAATG AAACAGACCGGCTGGTGCACTGGTGCCACGGCGCCCC GGGGGTCATCCACATGCTCATGCAGGCGTACAAG|GG GCTGTTACCCTTTGCTGTGGTAGGGAGTACAGATGAA GTGAAAGTTGGAAAAAGGATGGTCAGAGGCCGTCACT ACCCTTGGGGAGTTTTGCAAGTGGAAAATGAAAATCA CTGTGACTTCGTTAAGCTCCGAGATATGCTTCTTTGTAC CAATATGGAAAATCTAAAAGAAAAAACCCACACTCAG CACTATGAATGTTATAGGTACCAAAAACTGCAGAAAAT GGGCTTTACAGATGTGGGTCCAAACAACCAGCCAGTT AGTTTTCAAGAAATCTTTGAAGCCAAAAGACAAGAGTT CTATGATCAATGTCAGAGGGAAGAAGAAGAGTTGAAA CAGAGATTTATGCAGCGAGTCAAGGAGAAAGAAGCAA CATTTAAAGAAGCTGAAAAAGAGCTGCAGGACAAGTT CGAGCATCTTAAAATGATTCAACAGGAGGAGATAAGG AAGCTCGAGGAAGAGAAAAAACAACTGGAAGGAGAA ATCATAGATTTTTATAAAATGAAAGCTGCCTCCGAAGC ACTGCAGACTCAGCTGAGCACCGATACAAAGAAAGAC AAACATCGTAAGAAA G17512. 55268106 55863785 InFrame 8281 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-27- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 1837- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01A-01R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1850- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.2 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAG|CTGCAG GACAAGTTCGAGCATCTTAAAATGATTCAACAGGAGG AGATAAGGAAGCTCGAGGAAGAGAAAAAACAACTGG AAGGAGAAATCATAGATTTTTATAAAATGAAAGCTGCC TCCGAAGCACTGCAGACTCAGCTGAGCACCGATACAA AGAAAGACAAACATCGTAAGAAA NYU_A 1808661 1737458 InFrame 8282 ATGGGCGCCCCTGCCTGCGCCCTCGCGCTCTGCGTGGC CGTGGCCATCGTGGCCGGCGCCTCCTCGGAGTCCTTG GGGACGGAGCAGCGCGTCGTGGGGCGAGCGGCAGAA GTCCCGGGCCCAGAGCCCGGCCAGCAGGAGCAGTTG GTCTTCGGCAGCGGGGATGCTGTGGAGCTGAGCTGTC CCCCGCCCGGGGGTGGTCCCATGGGGCCCACTGTCTG GGTCAAGGATGGCACAGGGCTGGTGCCCTCGGAGCGT GTCCTGGTGGGGCCCCAGCGGCTGCAGGTGCTGAATG CCTCCCACGAGGACTCCGGGGCCTACAGCTGCCGGCA GCGGCTCACGCAGCGCGTACTGTGCCACTTCAGTGTGC GGGTGACAGACGCTCCATCCTCGGGAGATGACGAAGA CGGGGAGGACGAGGCTGAGGACACAGGTGTGGACAC AGGGGCCCCTTACTGGACACGGCCCGAGCGGATGGAC AAGAAGCTGCTGGCCGTGCCGGCCGCCAACACCGTCC GCTTCCGCTGCCCAGCCGCTGGCAACCCCACTCCCTCC ATCTCCTGGCTGAAGAACGGCAGGGAGTTCCGCGGCG AGCACCGCATTGGAGGCATCAAGCTGCGGCATCAGCA GTGGAGCCTGGTCATGGAAAGCGTGGTGCCCTCGGAC CGCGGCAACTACACCTGCGTCGTGGAGAACAAGTTTG GCAGCATCCGGCAGACGTACACGCTGGACGTGCTGGA GCGCTCCCCGCACCGGCCCATCCTGCAGGCGGGGCTG CCGGCCAACCAGACGGCGGTGCTGGGCAGCGACGTG GAGTTCCACTGCAAGGTGTACAGTGACGCACAGCCCC ACATCCAGTGGCTCAAGCACGTGGAGGTGAATGGCAG CAAGGTGGGCCCGGACGGCACACCCTACGTTACCGTG CTCAAGTCCTGGATCAGTGAGAGTGTGGAGGCCGACG TGCGCCTCCGCCTGGCCAATGTGTCGGAGCGGGACGG GGGCGAGTACCTCTGTCGAGCCACCAATTTCATAGGC GTGGCCGAGAAGGCCTTTTGGCTGAGCGTTCACGGGC CCCGAGCAGCCGAGGAGGAGCTGGTGGAGGCTGACG AGGCGGGCAGTGTGTATGCAGGCATCCTCAGCTACGG GGTGGGCTTCTTCCTGTTCATCCTGGTGGTGGCGGCTG TGACGCTCTGCCGCCTGCGCAGCCCCCCCAAGAAAGG CCTGGGCTCCCCCACCGTGCACAAGATCTCCCGCTTCC CGCTCAAGCGACAGGTGTCCCTGGAGTCCAACGCGTC CATGAGCTCCAACACACCACTGGTGCGCATCGCAAGG CTGTCCTCAGGGGAGGGCCCCACGCTGGCCAATGTCT CCGAGCTCGAGCTGCCTGCCGACCCCAAATGGGAGCT GTCTCGGGCCCGGCTGACCCTGGGCAAGCCCCTTGGG GAGGGCTGCTTCGGCCAGGTGGTCATGGCGGAGGCC ATCGGCATTGACAAGGACCGGGCCGCCAAGCCTGTCA CCGTAGCCGTGAAGATGCTGAAAGACGATGCCACTGA CAAGGACCTGTCGGACCTGGTGTCTGAGATGGAGATG ATGAAGATGATCGGGAAACACAAAAACATCATCAACC TGCTGGGCGCCTGCACGCAGGGCGGGCCCCTGTACGT GCTGGTGGAGTACGCGGCCAAGGGTAACCTGCGGGA GTTTCTgcgggcgcggcggcccccgggccTGGACTACTCCTTC GACACCTGCAAGCCGCCCGAGGAGCAGCTCACCTTCA AGGACCTGGTGTCCTGTGCCTACCAGGTGGCCCGGGG CATGGAGTACTTGGCCTCCCAGAAGTGCATCCACAGG GACCTGGCTGCCCGCAATGTGCTGGTGACCGAGGACA ACGTGATGAAGATCGCAGACTTCGGGCTGGCCCGGGA CGTGCACAACCTCGACTACTACAAGAAGACGACCAAC GGCCGGCTGCCCGTGAAGTGGATGGCGCCTGAGGCCT TGTTTGACCGAGTCTACACTCACCAGAGTGACGTCTGG TCCTTTGGGGTCCTGCTCTGGGAGATCTTCACGCTGGG GGGCTCCCCGTACCCCGGCATCCCTGTGGAGGAGCTCT TCAAGCTGCTGAAGGAGGGCCACCGCATGGACAAGCC CGCCAACTGCACACACGACCTGTACATGATCATGCGG GAGTGCTGGCATGCCGCGCCCTCCCAGAGGCCCACCTT CAAGCAGCTGGTGGAGGACCTGGACCGTGTCCTTACC GTGACGTCCACCGAC|TTTAAGGAGTCGGCCTTGAGG AAGCAGTCCTTATACCTCAAGTTCGACCCCCTCCTGAG GGACAGTCCTGGTAGACCAGTGCCCGTGGCCACCGAG ACCAGCAGCATGCACGGTGCAAATGAGACTCCCTCAG GACGTCCGCGGGAAGCCAAGCTTGTGGAGTTCGATTT CTTGGGAGCACTGGACATTCCTGTGCCAGGCCCACCCC CAGGTGTTCCCGCGCCTGGGGGCCCACCCCTGTCCACC GGACCTATAGTGGACCTGCTCCAGTACAGCCAGAAGG ACCTGGATGCAGTGGTAAAGGCGACACAGGAGGAGA ACCGGGAGCTGAGGAGCAGGTGTGAGGAGCTCCACG GGAAGAACCTGGAACTGGGGAAGATCATGGACAGGT TCGAAGAGGTTGTGTACCAGGCCATGGAGGAAGTTCA GAAGCAGAAGGAACTTTCCAAAGCTGAAATCCAGAAA GTTCTAAAAGAAAAAGACCAACTTACCACAGATCTGAA CTCCATGGAGAAGTCCTTCTCCGACCTCTTCAAGCGTTT TGAGAAACAGAAAGAGGTGATCGAGGGCTACCGCAA GAACGAAGAGTCACTGAAGAAGTGCGTGGAGGATTA CCTGGCAAGGATCACCCAGGAGGGCCAGAGGTACCAA GCCCTGAAGGCCCACGCGGAGGAGAAGCTGCAGCTG GCAAACGAGGAGATCGCCCAGGTCCGGAGCAAGGCC CAGGCGGAAGCGTTGGCCCTCCAGGCCAGCCTGAGGA AGGAGCAGATGCGCATCCAGTCGCTGGAGAAGACAGT GGAGCAGAAGACTAAAGAGAACGAGGAGCTGACCAG GATCTGCGACGACCTCATCTCCAAGATGGAGAAGATC G17814. 204951148 156844363 InFrame 8283 ATGGCCAGGCAGCCACCGCCGCCCTGGGTCCATGCAG TCGA-06- CCTTCCTCCTCTGCCTCCTCAGTCTTGGCGGAGCCATCG 5411- AAATTCCTATGGATCTGACGCAGCCGCCAACCATCACC 01A-01R- AAGCAGTCAGCGAAGGATCACATCGTGGACCCCCGTG 1849- ATAACATCCTGATTGAGTGTGAAGCAAAAGGGAACCC 01.4 TGCCCCCAGCTTCCACTGGACACGAAACAGCAGATTCT TCAACATCGCCAAGGACCCCCGGGTGTCCATGAGGAG GAGGTCTGGGACCCTGGTGATTGACTTCCGCAGTGGC GGGCGGCCGGAGGAATATGAGGGGGAATATCAGTGC TTCGCCCGCAACAAATTTGGCACGGCCCTGTCCAATAG GATCCGCCTGCAGGTGTCTAAATCTCCTCTGTGGCCCA AGGAAAACCTAGACCCTGTCGTGGTCCAAGAGGGCGC TCCTTTGACGCTCCAGTGCAACCCCCCGCCTGGACTTCC ATCCCCGGTCATCTTCTGGATGAGCAGCTCCATGGAGC CCATCACCCAAGACAAACGTGTCTCTCAGGGCCATAAC GGAGACCTATACTTCTCCAACGTGATGCTGCAGGACAT GCAGACCGACTACAGTTGTAACGCCCGCTTCCACTTCA CCCACACCATCCAGCAGAAGAACCCTTTCACCCTCAAG GTCCTCACCAACCACCCTTATAATGACTCGTCCTTAAGA AACCACCCTGACATGTACAGTGCCCGAGGAGTTGCAG AAAGAACACCAAGCTTCATGTATCCCCAGGGCACCGC GAGCAGCCAGATGGTGCTTCGTGGCATGGACCTCCTG CTGGAATGCATCGCCTCCGGGGTCCCAACACCAGACAT CGCATGGTACAAGAAAGGTGGGGACCTCCCATCTGAT AAGGCCAAGTTTGAGAACTTTAATAAGGCCCTGCGTAT CACAAATGTCTCTGAGGAAGACTCCGGGGAGTATTTCT GCCTGGCCTCCAACAAGATGGGCAGCATCCGGCACAC GATCTCGGTGAGAGTAAAGGCTGCTCCCTACTGGCTG GACGAACCCAAGAACCTTATTCTGGCTCCTGGCGAGG ATGGGAGACTGGTGTGTCGAGCCAATGGAAACCCCAA ACCCACTGTCCAGTGGATGGTGAATGGGGAACCTTTG CAATCGGCACCACCTAACCCAAACCGTGAGGTGGCCG GAGACACCATCATCTTCCGGGACACCCAGATCAGCAG CAGGGCTGTGTACCAGTGCAACACCTCCAACGAGCAT GGCTACCTGCTGGCCAACGCCTTTGTCAGTGTGCTGGA TGTGCCGCCTCGGATGCTGTCGCCCCGGAACCAGCTCA TTCGAGTGATTCTTTACAACCGGACGCGGCTGGACTGC CCTTTCTTTGGGTCTCCCATCCCCACACTGCGATGGTTT AAGAATGGGCAAGGAAGCAACCTGGATGGTGGCAAC TACCATGTTTATGAGAACGGCAGTCTGGAAATTAAGAT GATCCGCAAAGAGGACCAGGGCATCTACACCTGTGTC GCCACCAACATCCTGGGCAAAGCTGAAAACCAAGTCC GCCTGGAGGTCAAAGACCCCACCAGGATCTACCGGAT GCCCGAGGACCAGGTGGCCAGAAGGGGCACCACGGT GCAGCTGGAGTGTCGGGTGAAGCACGACCCCTCCCTG AAACTCACCGTCTCCTGGCTGAAGGATGACGAGCCGC TCTATATTGGAAACAGGATGAAGAAGGAAGACGACTC CCTGACCATCTTTGGGGTGGCAGAGCGGGACCAGGGC AGTTACACGTGTGTCGCCAGCACCGAGCTAGACCAAG ACCTGGCCAAGGCCTACCTCACCGTGCTAGCTGATCAG GCCACTCCAACTAACCGTTTGGCTGCCCTGCCCAAAGG ACGGCCAGACCGGCCCCGGGACCTGGAGCTGACCGAC CTGGCCGAGAGGAGCGTGCGGCTGACCTGGATCCCCG GGGATGCTAACAACAGCCCCATCACAGACTACGTCGTC CAGTTTGAAGAAGACCAGTTCCAACCTGGGGTCTGGC ATGACCATTCCAAGTACCCCGGCAGCGTTAACTCAGCC GTCCTCCGGCTGTCCCCGTATGTCAACTACCAGTTCCGT GTCATTGCCATCAACGAGGTTGGGAGCAGCCACCCCA GCCTCCCATCCGAGCGCTACCGAACCAGTGGAGCACC CCCCGAGTCCAATCCTGGTGACGTGAAGGGAGAGGG GACCAGAAAGAACAACATGGAGATCACGTGGACGCCC ATGAATGCCACCTCGGCCTTTGGCCCCAACCTGCGCTA CATTGTCAAGTGGAGGCGGAGAGAGACTCGAGAGGC CTGGAACAACGTCACAGTGTGGGGCTCTCGCTACGTG GTGGGGCAGACCCCAGTCTACGTGCCCTATGAGATCC GAGTCCAGGCTGAAAATGACTTCGGGAAGGGCCCTGA GCCAGAGTCCGTCATCGGTTACTCCGGAGAAGATT|AC ACTAACAGCACATCTGGAGACCCGGTGGAGAAGAAG GACGAAACACCTTTTGGGGTCTCGGTGGCTGTGGGCC TGGCCGTCTTTGCCTGCCTCTTCCTTTCTACGCTGCTCC TTGTGCTCAACAAATGTGGACGGAGAAACAAGTTTGG GATCAACCGCCCGGCTGTGCTGGCTCCAGAGGATGGG CTGGCCATGTCCCTGCATTTCATGACATTGGGTGGCAG CTCCCTGTCCCCCACCGAGGGCAAAGGCTCTGGGCTCC AAGGCCACATCATCGAGAACCCACAATACTTCAGTGAT GCCTGTGTTCACCACATCAAGCGCCGGGACATCGTGCT CAAGTGGGAGCTGGGGGAGGGCGCCTTTGGG AAGGT CTTCCTTGCTGAGTGCCACAACCTCCTGCCTGAGCAGG ACAAGATGCTGGTGGCTGTCAAGGCACTGAAGGAGGC GTCCGAGAGTGCTCGGCAGGACTTCCAGCGTGAGGCT GAGCTGCTCACCATGCTGCAGCACCAGCACATCGTGC GCTTCTTCGGCGTCTGCACCGAGGGCCGCCCCCTGCTC ATGGTCTTTGAGTATATGCGGCACGGGGACCTCAACC GCTTCCTCCGATCCCATGGACCTGATGCCAAGCTGCTG GCTGGTGGGGAGGATGTGGCTCCAGGCCCCCTGGGTC TGGGGCAGCTGCTGGCCGTGGCTAGCCAGGTCGCTGC GGGGATGGTGTACCTGGCGGGTCTGCATTTTGTGCAC CGGGACCTGGCCACACGCAACTGTCTAGTGGGCCAGG GACTGGTGGTCAAGATTGGTGATTTTGGCATGAGCAG GGATATCTACAGCACCGACTATTACCGTGTGGGAGGC CGCACCATGCTGCCCATTCGCTGGATGCCGCCCGAGA GCATCCTGTACCGTAAGTTCACCACCGAGAGCGACGT GTGGAGCTTCGGCGTGGTGCTCTGGGAGATCTTCACC TACGGCAAGCAGCCCTGGTACCAGCTCTCCAACACGG AGGCAATCGACTGCATCACGCAGGGACGTGAGTTGGA GCGGCCACGTGCCTGCCCACCAGAGGTCTACGCCATC ATGCGGGGCTGCTGGCAGCGGGAGCCCCAGCAACGC CACAGCATCAAGGATGTGCACGCCCGGCTGCAAGCCC TGGCCCAGGCACCTCCTGTCTACCTGGATGTCCTGGGC G17223. 55268106 55863785 InFrame 8284 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-06- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 0750- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01A-01R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1849- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.2 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAG|CTGCAG GACAAGTTCGAGCATCTTAAAATGATTCAACAGGAGG AGATAAGGAAGCTCGAGGAAGAGAAAAAACAACTGG AAGGAGAAATCATAGATTTTTATAAAATGAAAGCTGCC TCCGAAGCACTGCAGACTCAGCTGAGCACCGATACAA AGAAAGACAAACATCGTAAGAAA G17798. 55268106 55863785 InFrame 8285 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-32- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 5222- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01A-01R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1850- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.4 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAG|CTGCAG GACAAGTTCGAGCATCTTAAAATGATTCAACAGGAGG AGATAAGGAAGCTCGAGGAAGAGAAAAAACAACTGG AAGGAGAAATCATAGATTTTTATAAAATGAAAGCTGCC TCCGAAGCACTGCAGACTCAGCTGAGCACCGATACAA AGAAAGACAAACATCGTAAGAAA G17195. 69764755 58339411 InFrame 8286 ATGTTCAAGAGAATGGCCGAATTTGGGCCTGACTCCG TCGA-06- GCGGGAGAGTAAAGGGTGTTACTATCGTTAAACCAAT 0138- AGTTTACGGTAATGTTGCTCGGTATTTTGGAAAGAAAA 01A-02R- GAGAAGAAGATGGGCACACTCATCAGTGGACAGTATA 1849- TGTGAAACCATATAGAAATGAGGATATGTCAGCATAT 01.2 GTGAAGAAAATCCAGTTTAAATTACATGAAAGCTATG GCAATCCTTTAAGAGTTGTTACTAAACCTCCATATGAA ATTACTGAAACAGGATGGGGTGAATTCGAAATAATCA TCAAAATATTTTTCATTGACCCTAATGAAAGACCTGTAA CCCTGTATCATTTGCTAAAGCTGTTTCAATCAGACACCA ATGCAATGCTGGGGAAAAAGACAGTGGTTTCAGAGTT CTATGATGAAATGATATTTCAAGACCCAACAGCAATGA TGCAACAATTATTGACAACATCTCGTCAGCTAACATTA GGAGCCTATAAGCATGAAACAGAAT|ATCCATATGTCA AACTTCTGCTTGATGCTATGAAACACTCAGGTTGTGCT GTTAACAAAGATAGACACTTTTCTTGCGAAGACTGTAA TGGAAATGTCAGTGGAGGTTTTGATGCTTCAACATCTC AGATAGTTTTGTGCCAGAATAATATCCATAATCAGGCC CATATGAACAGAGTGGTCACACACGAGCTTATTCATGC ATTTGATCATTGTCGTGCCCATGTCGACTGGTTCACCA ACATCAGACATTTGGCGTGCTCAGAGGTTCGAGCTGCT AACCTTAGTGGAGACTGCTCACTTGTCAATGAAATATT CAGGTTACATTTTGGATTAAAACAACACCACCAGACTT GTGTGCGAGACAGAGCCACTCTTTCTATCCTGGCTGTT AGGAATATCAGCAAAGAAGTAGCTAAAAAGGCTGTTG ATGAAGTTTTTGAATCTTGTTTCAATGACCATGAACCTT TTGGAAGGATCCCACATAACAAGACTTATGCAAGATAT GCTCACAGAGACTTTGAAAACCGTGATCGGTATTATTC AAATATA G17803. 1808661 1739325 InFrame 8287 ATGGGCGCCCCTGCCTGCGCCCTCGCGCTCTGCGTGGC 8287 CGTGGCCATCGTGGCCGGCGCCTCCTCGGAGTCCTTG TCGA-76- GGGACGGAGCAGCGCGTCGTGGGGCGAGCGGCAGAA 4925- GTCCCGGGCCCAGAGCCCGGCCAGCAGGAGCAGTTG 01A-01R- GTCTTCGGCAGCGGGGATGCTGTGGAGCTGAGCTGTC 1850- CCCCGCCCGGGGGTGGTCCCATGGGGCCCACTGTCTG 01.4 GGTCAAGGATGGCACAGGGCTGGTGCCCTCGGAGCGT GTCCTGGTGGGGCCCCAGCGGCTGCAGGTGCTGAATG CCTCCCACGAGGACTCCGGGGCCTACAGCTGCCGGCA GCGGCTCACGCAGCGCGTACTGTGCCACTTCAGTGTGC GGGTGACAGACGCTCCATCCTCGGGAGATGACGAAGA CGGGGAGGACGAGGCTGAGGACACAGGTGTGGACAC AGGGGCCCCTTACTGGACACGGCCCGAGCGGATGGAC AAGAAGCTGCTGGCCGTGCCGGCCGCCAACACCGTCC GCTTCCGCTGCCCAGCCGCTGGCAACCCCACTCCCTCC ATCTCCTGGCTGAAGAACGGCAGGGAGTTCCGCGGCG AGCACCGCATTGGAGGCATCAAGCTGCGGCATCAGCA GTGGAGCCTGGTCATGGAAAGCGTGGTGCCCTCGGAC CGCGGCAACTACACCTGCGTCGTGGAGAACAAGTTTG GCAGCATCCGGCAGACGTACACGCTGGACGTGCTGGA GCGCTCCCCGCACCGGCCCATCCTGCAGGCGGGGCTG CCGGCCAACCAGACGGCGGTGCTGGGCAGCGACGTG GAGTTCCACTGCAAGGTGTACAGTGACGCACAGCCCC ACATCCAGTGGCTCAAGCACGTGGAGGTGAATGGCAG CAAGGTGGGCCCGGACGGCACACCCTACGTTACCGTG CTCAAGTCCTGGATCAGTGAGAGTGTGGAGGCCGACG TGCGCCTCCGCCTGGCCAATGTGTCGGAGCGGGACGG GGGCGAGTACCTCTGTCGAGCCACCAATTTCATAGGC GTGGCCGAGAAGGCCTTTTGGCTGAGCGTTCACGGGC CCCGAGCAGCCGAGGAGGAGCTGGTGGAGGCTGACG AGGCGGGCAGTGTGTATGCAGGCATCCTCAGCTACGG GGTGGGCTTCTTCCTGTTCATCCTGGTGGTGGCGGCTG TGACGCTCTGCCGCCTGCGCAGCCCCCCCAAGAAAGG CCTGGGCTCCCCCACCGTGCACAAGATCTCCCGCTTCC CGCTCAAGCGACAGGTGTCCCTGGAGTCCAACGCGTC CATGAGCTCCAACACACCACTGGTGCGCATCGCAAGG CTGTCCTCAGGGGAGGGCCCCACGCTGGCCAATGTCT CCGAGCTCGAGCTGCCTGCCGACCCCAAATGGGAGCT GTCTCGGGCCCGGCTGACCCTGGGCAAGCCCCTTGGG GAGGGCTGCTTCGGCCAGGTGGTCATGGCGGAGGCC ATCGGCATTGACAAGGACCGGGCCGCCAAGCCTGTCA CCGTAGCCGTGAAGATGCTGAAAGACGATGCCACTGA CAAGGACCTGTCGGACCTGGTGTCTGAGATGGAGATG ATGAAGATGATCGGGAAACACAAAAACATCATCAACC TGCTGGGCGCCTGCACGCAGGGCGGGCCCCTGTACGT GCTGGTGGAGTACGCGGCCAAGGGTAACCTGCGGGA GTTTCTgcgggcgcggcggcccccgggccTGGACTACTCCTTC GACACCTGCAAGCCGCCCGAGGAGCAGCTCACCTTCA AGGACCTGGTGTCCTGTGCCTACCAGGTGGCCCGGGG CATGGAGTACTTGGCCTCCCAGAAGTGCATCCACAGG GACCTGGCTGCCCGCAATGTGCTGGTGACCGAGGACA ACGTGATGAAGATCGCAGACTTCGGGCTGGCCCGGGA CGTGCACAACCTCGACTACTACAAGAAGACGACCAAC GGCCGGCTGCCCGTGAAGTGGATGGCGCCTGAGGCCT TGTTTGACCGAGTCTACACTCACCAGAGTGACGTCTGG TCCTTTGGGGTCCTGCTCTGGGAGATCTTCACGCTGGG GGGCTCCCCGTACCCCGGCATCCCTGTGGAGGAGCTCT TCAAGCTGCTGAAGGAGGGCCACCGCATGGACAAGCC CGCCAACTGCACACACGACCTGTACATGATCATGCGG GAGTGCTGGCATGCCGCGCCCTCCCAGAGGCCCACCTT CAAGCAGCTGGTGGAGGACCTGGACCGTGTCCTTACC GTGACGTCCACCGAC|GTGCCAGGCCCACCCCCAGGT GTTCCCGCGCCTGGGGGCCCACCCCTGTCCACCGGACC TATAGTGGACCTGCTCCAGTACAGCCAGAAGGACCTG GATGCAGTGGTAAAGGCGACACAGGAGGAGAACCGG GAGCTGAGGAGCAGGTGTGAGGAGCTCCACGGGAAG AACCTGGAACTGGGGAAGATCATGGACAGGTTCGAAG AGGTTGTGTACCAGGCCATGGAGGAAGTTCAGAAGCA GAAGGAACTTTCCAAAGCTGAAATCCAGAAAGTTCTA AAAGAAAAAGACCAACTTACCACAGATCTGAACTCCAT GGAGAAGTCCTTCTCCGACCTCTTCAAGCGTTTTGAGA AACAGAAAGAGGTGATCGAGGGCTACCGCAAGAACG AAGAGTCACTGAAGAAGTGCGTGGAGGATTACCTGGC AAGGATCACCCAGGAGGGCCAGAGGTACCAAGCCCTG AAGGCCCACGCGGAGGAGAAGCTGCAGCTGGCAAAC GAGGAGATCGCCCAGGTCCGGAGCAAGGCCCAGGCG GAAGCGTTGGCCCTCCAGGCCAGCCTGAGGAAGGAGC AGATGCGCATCCAGTCGCTGGAGAAGACAGTGGAGCA GAAGACTAAAGAGAACGAGGAGCTGACCAGGATCTG CGACGACCTCATCTCCAAGATGGAGAAGATC NYU_B 7388176 7604059 InFrame 8288 ATGCACGGGGGTGGCCCCCCCTCGGGGGACAGCGCAT GCCCGCTGCGCACCATCAAGAGAGTCCAGTTCGGAGT CCTGAGTCCGGATGAACTG|GTCCCTGTCCTTCGAATG GTGGAAGGTGATACCATCTATGATTACTGCTGGTATTC TCTGATGTCCTCAGCCCAGCCAGACACCTCCTACGTGG CCAGCAGCAGCCGGGAGAACCCGATTCATATCTGGGA CGCATTCACTGGAGAGCTCCGGGCTTCCTTTCGCGCCT ACAACCACCTGGATGAGCTGACGGCAGCCCATTCGCTC TGCTTCTCCCCGGATGGCTCCCAGCTCTTCTGTGGCTTC AACCGGACTGTGCGTGTTTTTTCCACGGCCCGGCCTGG CCGAGACTGCGAGGTCCGAGCCACATTTGCAAAAAAG CAGGGCCAGAGCGGCATCATCTCCTGCATAGCCTTCAG CCCAGCCCAGCCCCTCTATGCCTGTGGCTCCTACGGCC GCTCCCTGGGTCTGTATGCCTGGGATGATGGCTCCCCT CTCGCCTTGCTGGGAGGGCACCAAGGGGGCATCACCC ACCTCTGCTTTCATCCCGATGGCAACCGCTTCTTCTCAG GAGCCCGCAAGGATGCTGAGCTCCTGTGCTGGGATCT CCGGCAGTCTGGTTACCCACTGTGGTCCCTGGGTCGAG AGGTGACCACCAATCAGCGCATCTACTTCGATCTGGAC CCGACCGGGCAGTTCCTAGTGAGTGGCAGCACGAGCG GGGCTGTCTCTGTGTGGGACACGGACGGGCCTGGCAA TGATGGGAAGCCGGAGCCCGTGTTGAGTTTTCTGCCCC AGAAGGACTGCACCAATGGCGTGAGCCTGCACCCTAG CCTGCCTCTCCTGGCCACTGCCTCCGGTCAGCGTGTGT TTCCTGAGCCCACAGAGAGTGGGGACGAAGGAGAGG AGCTGGGCCTTCCCTTGCTCTCCACGCGCCACGTCCAC CTTGAATGTCGGCTTCAGCTCTGGTGGTGTGGGGGGG CGCCAGACTCCAGCATCCCTGATGATCACCAGGGCGA GAAAGGGCAGGGAGGAACGGAGGGAGGTGTGGGTG AGCTGATA G17507. 55268106 55863785 InFrame 8289 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-28- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 1747- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01C-01R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1850- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.2 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAG|CTGCAG GACAAGTTCGAGCATCTTAAAATGATTCAACAGGAGG AGATAAGGAAGCTCGAGGAAGAGAAAAAACAACTGG AAGGAGAAATCATAGATTTTTATAAAATGAAAGCTGCC TCCGAAGCACTGCAGACTCAGCTGAGCACCGATACAA AGAAAGACAAACATCGTAAGAAA G17469. 73604248 74173110 InFrame 8290 ATGGCGGACTTCGACACCTACGACGATCGGGCCTACA TCGA-06- GCAGCTTCGGCGGCGGCAGAGGGTCCCGCGGCAGTG 2557- CTGGTGGCCATGGTTCCCGTAGCCAGAAGGAGTTGCC 01A-01R- CACAGAGCCCCCCTACACAGCATACGTAGGAAATCTAC 1849- CTTTCAATACGGTTCAGGGCGACATAGATGCTATCTTT 01.2 AAGGATCTCAGCATAAGGAGTGTACGGCTAGTCAGAG ACAAAGACACAGATAAATTTAAAGGATTCTGCTATGTA GAATTCGATGAAGTGGATTCCCTTAAGGAAGCCTTGAC ATACGATGGTGCACTGTTGGGCGATCGGTCACTTCGTG TGGACATTGCAGAAGGCAGAAAACAAGATAAAGGTG GCTTTGGATTCAGAAAAGGTGGACCAGATGACAGAG| AAATAAAAGAGACTGATGGAAGCTCTCAGATCAAGCA AGAACCAGACCCCACGTGG G17785. 32903023 3440021 InFrame 8291 ATGTTAACCATGAGCGTGACACTTTCCCCCCTGAGGTC TCGA-06- ACAGGACCTGGATCCCATGGCTACTGATGCTTCACCCA 5413- TGGCCATCAACATGACACCCACTGTGGAGCAGGGTGA 01A-01R- GGGAGAAGAGGCAATGAAGGACATGGACTCTGACCA 1849- GCAGTATGAAAAGCCACCCCCACTACACACAGGGGCT 01.4 GACTGGAAGATTGTCCTCCACTTACCTGAAATTGAGAC CTGGCTCCGGATGACCTCAGAGAGGGTCCGAGACCTA ACCTATTCAGTCCAGCAGGATTCGGACAGCAAGCATGT GGATGTACATCTAGTTCAACTAAAG|GCAATGGTGGCT TGCTATCCGGGAAATGGAACAGGTTATGTTCGCCACGT GGACAACCCCAACGGTGATGGTCGCTGCATCACCTGC ATCTACTATCTGAACAAGAATTGGGATGCCAAGCTACA TGGTGGGATCCTGCGGATATTTCCAGAGGGGAAATCA TTCATAGCAGATGTGGAGCCCATTTTTGACAGACTCCT GTTCTTCTGGTCAGATCGTAGGAACCCACACGAAGTGC AGCCCTCTTACGCAACCAGATATGCTATGACTGTCTGG TACTTTGATGCTGAAGAAAGGGCAGAAGCCAAAAAGA AATTCAGGAATTTAACTAGGAAAACTGAATCTGCCCTC ACTGAAGAC G17467. 102606509 12856191 InFrame 8292 ATGGCGACGGAGGGAGGAGGGAAGGAGATGAACGA TCGA-14- GATTAAGACCCAATTCACCACCCGGGAAGGTCTGTACA 0736- AGCTGCTGCCGCACTCGGAGTACAGCCGGCCCAACCG 02A-01R- GGTGCCCTTCAACTCGCAGGGATCCAACCCTGTCCGCG 2005- TCTCCTTCGTAAACCTCAACGACCAGTCTGGCAACGGC 01.2 GACCGCCTCTGCTTCAATGTGGGCCGGGAGCTGTACTT CTATATCTACAAGGGGGTCCGCAAG|GAGATTGACCCC AGCCTGGGCGTGGCGGAGCTGCCTGACGAGTTCTTCG AGGAGGACAACATGCTGAGCATGGGCAAGAAGATGA TGCAGGAGGCCATGAGCGCATTTCCCGGCATCGATGA GGCCATGAGCTATGCCGAGGTCATGAGGCTGGTGAAG GGCATGAACTTCTCGGTGGTGGTATTTGACACGGCACC CACGGGCCACACCCTGAGGCTGCTCAACTTCCCCACCA TCGTGGAGCGGGGCCTGGGCCGGCTTATGCAGATCAA GAACCAGATCAGCCCTTTCATCTCACAGATGTGCAACA TGCTGGGCCTGGGGGACATGAACGCAGACCAGCTGGC CTCCAAGCTGGAGGAGACGCTGCCCGTCATCCGCTCA GTCAGCGAACAGTTCAAGGACCCTGAGCAGACAACTT TCATCTGCGTATGCATTGCTGAGTTCCTGTCCCTGTATG AGACAGAGAGGCTGATCCAGGAGCTGGCCAAGTGCA AGATTGACACACACAATATAATTGTCAACCAGCTCGTC TTCCCCGACCCCGAGAAGCCCTGCAAGATGTGTGAGG CCCGTCACAAGATCCAGGCCAAGTATCTGGACCAGAT GGAGGACCTGTATGAAGACTTCCACATCGTGAAGCTG CCGCTGTTACCCCATGAGGTGCGGGGGGCAGACAAGG TCAACACCTTCTCGGCCCTCCTCCTGGAGCCCTACAAG CCCCCCAGTGCCCAG GBM- 22160139 58166800 InFrame 8293 atggcggcggcggcggcggcggGCGCGGGCCCGGAGATGGT CUMC3316_L1 CCGCGGGCAGGTGTTCGACGTGGGGCCGCGCTACACC AACCTCTCGTACATCGGCGAGGGCGCCTACGGCATGG TGTGCTCTGCTTATGATAATGTCAACAAAGTTCGAGTA GCTATCAAGAAAATCAGCCCCTTTGAGCACCAGACCTA CTGCCAGAGAACCCTGAGGGAGATAAAAATCTTACTG CGCTTCAGACATGAGAACATCATTGGAATCAATGACAT TATTCGAGCACCAACCATCGAGCAAATGAAAGATGTAT ATATAGTACAGGACCTCATGGAAACAGATCTTTACAAG CTCTTGAAGACACAACACCTCAGCAATGACCATATCTG CTATTTTCTCTACCAGATCCTCAGAGGGTTAAAATATAT CCATTCAGCTAACGTTCTGCACCGTGACCTCAAGCCTTC CAACCTGCTGCTCAACACCACCTGTGATCTCAAG|GCC CTGAGCCTGTGCAATTATTTCGAGAGTCAAAATGTGGA TTTCCGAGGCAAGAAGGTGATCGAACTGGGTGCGGG GACAGGCATCGTGGGGATCTTGGCAGCGCTGCAGGG GGGGGATGTTACCATCACTGACCTGCCCCTGGCCCTAG AACAGATCCAGGGCAACGTCCAGGCCAATGTGCCAGC TGGAGGCCAGGCCCAGGTGCGTGCCTTGTCCTGGGGG ATTGACCATCATGTCTTCCCTGCAAACTATGACCTGGT GCTGGGGGCTGATATCGTGTACCTGGAACCCACCTTCC CTCTGCTGCTGGGGACCCTCCAACACCTGTGCAGGCCC CATGGCACCATCTATCTGGCCTCCAAGATGAGAAAGG AGCATGGGACAGAGAGCTTCTTTCAGCACCTCCTGCCC CAGCATTTCCAACTGGAGCTGGCTCAGCGGGATGAGG ATGAAAATGTCAACATCTATAGGGCCAGGCACAGGGA ACCAAGACCTGCT G17663. 156628525 156844698 InFrame 8294 ATGGCCCAGCTGTTCCTGCCCCTGCTGGCAGCCCTGGT TCGA-19- CCTGGCCCAGGCTCCTGCAGCTTTAGCAGATGTTCTGG 2619- AAGGAGACAGCTCAGAGGACCGCGCTTTTCGCGTGCG 01A-01R- CATCGCGGGCGACGCGCCACTGCAGGGCGTGCTCGGC 1850- GGCGCCCTCACCATCCCTTGCCACGTCCACTACCTGCG 01.2 GCCACCGCCGAGCCGCCGGGCTGTGCTGGGCTCTCCG CGGGTCAAGTGGACTTTCCTGTCCCGGGGCCGGGAGG CAGAGGTGCTGGTGGCGCGGGGAGTGCGCGTCAAGG TGAACGAGGCCTACCGGTTCCGCGTGGCACTGCCTGC GTACCCAGCGTCGCTCACCGACGTCTCCCTGGCGCTGA GCGAGCTGCGCCCCAACGACTCAGGTATCTATCGCTGT GAGGTCCAGCACGGCATCGATGACAGCAGCGACGCTG TGGAGGTCAAGGTCAAAGGGGTCGTCTTTCTCTACCG AGAGGGCTCTGCCCGCTATGCTTTCTCCTTTTCTGGGG CCCAGGAGGCCTGTGCCCGCATTGGAGCCCACATCGC CACCCCGGAGCAGCTCTATGCCGCCTACCTTGGGGGCT ATGAGCAATGTGATGCTGGCTGGCTGTCGGATCAGAC CGTGAGGTATCCCATCCAGACCCCACGAGAGGCCTGTT ACGGAGACATGGATGGCTTCCCCGGGGTCCGGAACTA TGGTGTGGTGGACCCGGATGACCTCTATGATGTGTACT GTTATGCTGAAGACCTAAATGGAGAACTGTTCCTGGGT GACCCTCCAGAGAAGCTGACATTGGAGGAAGCACGG GCGTACTGCCAGGAGCGGGGTGCAGAGATTGCCACCA CGGGCCAACTGTATGCAGCCTGGGATGGTGGCCTGGA CCACTGCAGCCCAGGGTGGCTAGCTGATGGCAGTGTG CGCTACCCCATCGTCACACCCAGCCAGCGCTGTGGTGG GGGCTTGCCTGGTGTCAAGACTCTCTTCCTCTTCCCCAA CCAGACTGGCTTCCCCAATAAGCACAGCCGCTTCAACG TCTACTGCTTCCGAGACTCGGCCCAGCCTTCTGCCATCC CTGAGgcctccaacccagcctccaacccagcctcTGATGGACTA GAGGCTATCGTCACAGTGACAGAGACCCTGGAGGAAC TGCAGCTGCCTCAGGAAGCCACAGAGAGTGAATCCCG TGGGGCCATCTACTCCATCCCCATCATGGAGGACGGA GGAGGTGGAAGCTCCACTCCAGAAGACCCAGCAGAG GCCCCTAGGACGCTCCTAGAATTTGAAACACAATCCAT GGTACCGCCCACGGGGTTCTCAGAAGAGGAAGGTAA GGCATTggaggaagaagagaaatatgaagatgaagaagagaaag aggaggaagaagaagaggaggaggtggaggatgaggCTCTGTGG GCATGGCCCAGCGAGCTCAGCAGCCCGGGCCCTGAGG CCTCTCTCCCCACTGAGCCAGCAGCCCAGGAGGAGTCA CTCTCCCAGGCGCCAGCAAGGGCAGTCCTGCAGCCTG GTGCATCACCACTTCCTGATGGAGAGTCAGAAGCTTCC AGGCCTCCAAGGGTCCATGGACCACCTACTGAGACTCT GCCCACTCCCAGGGAGAGGAACCTAGCATCCCCATCA CCTTCCACTCTGGTTGAGGCAAGAGAGGTGGGGGAGG CAACTGGTGGTCCTGAGCTATCTGGGGTCCCTCGAGG AGAGAGCGAGGAGACAGGAAGCTCCGAGGGTGCCCC TTCCCTGCTTCCAGCCACACGGGCCCCTGAGGGTACCA GGGAGCTGGAGGCCCCCTCTGAAGATAATTCTGGAAG AACTGCCCCAGCAGGGACCTCAGTGCAGGCCCAGCCA GTGCTGCCCACTGACAGCGCCAGCCGAGGTGGAGTGG CCGTGGTCCCCGCATCAGGTGACTGTGTCCCCAGCCCC TGCCACAATGGTGGGACATGCTTGGAGGAGGAGGAA GGGGTCCGCTGCCTATGTCTGCCTGGCTATGGGGGGG ACCTGTGCGATGTTGGCCTCCGCTTCTGCAACCCCGGC TGGGACGCCTTCCAGGGCGCCTGCTACAAGCACTTTTC CACACGAAGGAGCTGGGAGGAGGCAGAGACCCAGTG CCGGATGTACGGCGCGCATCTGGCCAGCATCAGCACA CCCGAGGAACAGGACTTCATCAACAACCGGTACCGGG AGTACCAGTGGATCGGACTCAACGACAGGACCATCGA AGGCGACTTCTTGTGGTCGGATGGCGTCCCCCTGCTCT ATGAGAACTGGAACCCTGGGCAGCCTGACAGCTACTT CCTGTCTGGAGAGAACTGCGTGGTCATGGTGTGGCAT GATCAGGGACAATGGAGTGACGTGCCCTGCAACTACC ACCTGTCCTACACCTGCAAGATGGGGCTGGTGTCCTGT GGGCCGCCACCGGAGCTGCCCCTGGCTCAAGTGTTCG GCCGCCCACGGCTGCGCTATGAGGTGGACACTGTGCT TCGCTACCGGTGCCGGGAAGGACTGGCCCAGCGCAAT CTGCCGCTGATCCGATGCCAAGAGAACGGTCGTTGGG AGGCCCCCCAGATCTCCTGTGTGCCCAGAAGACCT|GT CTCGGTGGCTGTGGGCCTGGCCGTCTTTGCCTGCCTCT TCCTTTCTACGCTGCTCCTTGTGCTCAACAAATGTGGAC GGAGAAACAAGTTTGGGATCAACCGCCCGGCTGTGCT GGCTCCAGAGGATGGGCTGGCCATGTCCCTGCATTTCA TGACATTGGGTGGCAGCTCCCTGTCCCCCACCGAGGG CAAAGGCTCTGGGCTCCAAGGCCACATCATCGAGAAC CCACAATACTTCAGTGATGCCTGTGTTCACCACATCAA GCGCCGGGACATCGTGCTCAAGTGGGAGCTGGGGGA GGGCGCCTTTGGGAAGGTCTTCCTTGCTGAGTGCCACA ACCTCCTGCCTGAGCAGGACAAGATGCTGGTGGCTGT CAAGGCACTGAAGGAGGCGTCCGAGAGTGCTCGGCA GGACTTCCAGCGTGAGGCTGAGCTGCTCACCATGCTG CAGCACCAGCACATCGTGCGCTTCTTCGGCGTCTGCAC CGAGGGCCGCCCCCTGCTCATGGTCTTTGAGTATATGC GGCACGGGGACCTCAACCGCTTCCTCCGATCCCATGGA CCTGATGCCAAGCTGCTGGCTGGTGGGGAGGATGTGG CTCCAGGCCCCCTGGGTCTGGGGCAGCTGCTGGCCGT GGCTAGCCAGGTCGCTGCGGGGATGGTGTACCTGGCG GGTCTGCATTTTGTGCACCGGGACCTGGCCACACGCAA CTGTCTAGTGGGCCAGGGACTGGTGGTCAAGATTGGT GATTTTGGCATGAGCAGGGATATCTACAGCACCGACT ATTACCGTGTGGGAGGCCGCACCATGCTGCCCATTCGC TGGATGCCGCCCGAGAGCATCCTGTACCGTAAGTTCAC CACCGAGAGCGACGTGTGGAGCTTCGGCGTGGTGCTC TGGGAGATCTTCACCTACGGCAAGCAGCCCTGGTACC AGCTCTCCAACACGGAGGCAATCGACTGCATCACGCA GGGACGTGAGTTGGAGCGGCCACGTGCCTGCCCACCA GAGGTCTACGCCATCATGCGGGGCTGCTGGCAGCGGG AGCCCCAGCAACGCCACAGCATCAAGGATGTGCACGC CCGGCTGCAAGCCCTGGCCCAGGCACCTCCTGTCTACC TGGATGTCCTGGGC G17203. 54825188 55224226 InFrame 8295 ATGGATCAGGTAATGCAGTTTGTTGAGCCAAGTCGGC TCGA-06- AGTTTGTAAAGGACTCCATTCGGCTGGTTAAAAGATGC 0211- ACTAAACCTGATAGAAAAG|TGTGTAACGGAATAGGT 02A-02R- ATTGGTGAATTTAAAGACTCACTCTCCATAAATGCTAC 2005- GAATATTAAACACTTCAAAAACTGCACCTCCATCAGTG 01.2 GCGATCTCCACATCCTGCCGGTGGCATTTAGGGGTGAC TCCTTCACACATACTCCTCCTCTGGATCCACAGGAACTG GATATTCTGAAAACCGTAAAGGAAATCACAGGGTTTTT GCTGATTCAGGCTTGGCCTGAAAACAGGACGGACCTC CATGCCTTTGAGAACCTAGAAATCATACGCGGCAGGA CCAAGCAACATGGTCAGTTTTCTCTTGCAGTCGTCAGC CTGAACATAACATCCTTGGGATTACGCTCCCTCAAGGA GATAAGTGATGGAGATGTGATAATTTCAGGAAACAAA AATTTGTGCTATGCAAATACAATAAACTGGAAAAAACT GTTTGGGACCTCCGGTCAGAAAACCAAAATTATAAGC AACAGAGGTGAAAACAGCTGCAAGGCCACAGGCCAG GTCTGCCATGCCTTGTGCTCCCCCGAGGGCTGCTGGG GCCCGGAGCCCAGGGACTGCGTCTCTTGCCGGAATGT CAGCCGAGGCAGGGAATGCGTGGACAAGTGCAACCTT CTGGAGGGTGAGCCAAGGGAGTTTGTGGAGAACTCTG AGTGCATACAGTGCCACCCAGAGTGCCTGCCTCAGGC CATGAACATCACCTGCACAGGACGGGGACCAGACAAC TGTATCCAGTGTGCCCACTACATTGACGGCCCCCACTG CGTCAAGACCTGCCCGGCAGGAGTCATGGGAGAAAAC AACACCCTGGTCTGGAAGTACGCAGACGCCGGCCATG TGTGCCACCTGTGCCATCCAAACTGCACCTACGGATGC ACTGGGCCAGGTCTTGAAGGCTGTCCAACGAATGGGC CTAAGATCCCGTCCATCGCCACTGGGATGGTGGGGGC CCTCCTCTTGCTGCTGGTGGTGGCCCTGGGGATCGGCC TCTTCATGCGAAGGCGCCACATCGTTCGGAAGCGCAC GCTGCGGAGGCTGCTGCAGGAGAGGGAGCTTGTGGA GCCTCTTACACCCAGTGGAGAAGCTCCCAACCAAGCTC TCTTGAGGATCTTGAAGGAAACTGAATTCAAAAAGATC AAAGTGCTGGGCTCCGGTGCGTTCGGCACGGTGTATA AGGGACTCTGGATCCCAGAAGGTGAGAAAGTTAAAAT TCCCGTCGCTATCAAGGAATTAAGAGAAGCAACATCTC CGAAAGCCAACAAGGAAATCCTCGATGAAGCCTACGT GATGGCCAGCGTGGACAACCCCCACGTGTGCCGCCTG CTGGGCATCTGCCTCACCTCCACCGTGCAGCTCATCAC GCAGCTCATGCCCTTCGGCTGCCTCCTGGACTATGTCC GGGAACACAAAGACAATATTGGCTCCCAGTACCTGCTC AACTGGTGTGTGCAGATCGCAAAGGGCATGAACTACT TGGAGGACCGTCGCTTGGTGCACCGCGACCTGGCAGC CAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAG ATCACAGATTTTGGGCTGGCCAAACTGCTGGGTGCGG AAGAGAAAGAATACCATGCAGAAGGAGGCAAAGTGC CTATCAAGTGGATGGCATTGGAATCAATTTTACACAGA ATCTATACCCACCAGAGTGATGTCTGGAGCTACGGGG TGACTGTTTGGGAGTTGATGACCTTTGGATCCAAGCCA TATGACGGAATCCCTGCCAGCGAGATCTCCTCCATCCT GGAGAAAGGAGAACGCCTCCCTCAGCCACCCATATGT ACCATCGATGTCTACATGATCATGGTCAAGTGCTGGAT GATAGACGCAGATAGTCGCCCAAAGTTCCGTGAGTTG ATCATCGAATTCTCCAAAATGGCCCGAGACCCCCAGCG CTACCTTGTCATTCAGGGGGATGAAAGAATGCATTTGC CAAGTCCTACAGACTCCAACTTCTACCGTGCCCTGATG GATGAAGAAGACATGGACGACGTGGTGGATGCCGAC GAGTACCTCATCCCACAGCAGGGCTTCTTCAGCAGCCC CTCCACGTCACGGACTCCCCTCCTGAGCTCTCTGAGTG CAACCAGCAACAATTCCACCGTGGCTTGCATTGATAGA AATGGGCTGCAAAGCTGTCCCATCAAGGAAGACAGCT TCTTGCAGCGATACAGCTCAGACCCCACAGGCGCCTTG ACTGAGGACAGCATAGACGACACCTTCCTCCCAGTGCC TGaATACATAAACCAGTCCGTTCCCAAAAGGCCCGCTG GCTCTGTGCAGAATCCTGTCTATCACAATCAGCCTCTG AACCCCGCGCCCAGCAGAGACCCACACTACCAGGACC CCCACAGCACTGCAGTGGGCAACCCCGAGTATCTCAAC ACTGTCCAGCCCACCTGTGTCAACAGCACATTCGACAG CCCTGCCCACTGGGCCCAGAAAGGCAGCCACCAAATT AGCCTGGACAACCCTGACTACCAGCAGGACTTCTTTCC CAAGGAAGCCAAGCCAAATGGCATCTTTAAGGGCTCC ACAGCTGAAAATGCAGAATACCTAAGGGTCGCGCCAC AAAGCAGTGAATTTATTGGAGCA G17784. 9675963 9731644 InFrame 8296 ATGAGGCAGTCTCTCCTATTCCTGACCAGCGTGGTTCC TCGA-76- TTTCGTGCTGGCGCCGCGACCTCCGGATGACCCGGGC 4929- TTCGGCCCCCACCAGAGACTCGAGAAGCTTGATTCTTT 01A-01R- GCTCTCAGACTACGATATTCTCTCTTTATCTAATATCCA 1850- GCAGCATTCGGTAAGAAAAAGAGATCTACAGACTTCA 01.4 ACACATGTAGAAACACTACTAACTTTTTCAGCTTTGAA AAGGCATTTTAAATTATACCTGACATCAAGTACTGAAC GTTTTTCACAAAATTTCAAGGTCGTGGTGGTGGATGGT AAAAACGAAAGCGAGTACACTGTAAAATGGCAGGACT TCTTCACTGGACACGTGGTTGGTGAGCCTGACTCTAGG GTTCTAGCCCACATAAGAGATGATGATGTTATAATCAG AATCAACACAGATGGGGCCGAATATAACATAGAG|GA ATTGTTGGATAAATATTTAATAGCCAATGCAACTAATC CAGAGAGTAAGGTCTTCTATCTGAAAATGAAGGGTGA TTACTTCCGGTACCTTGCTGAAGTTGCGTGTGGTGATG ATCGAAAACAAACGATAGATAATTCCCAAGGAGCTTAC CAAGAGGCATTTGATATAAGCAAGAAAGAGATGCAAC CCACACACCCAATCCGCCTGGGGCTTGCTCTTAACTTTT CTGTATTTTACTATGAGATTCTTAATAACCCAGAGCTTG CCTGCACGCTGGCTAAAACGGCTTTTGATGAGGCCATT GCTGAACTTGATACACTGAATGAAGACTCATACAAAG ACAGCACCCTCATCATGCAGTTGCTTAGAGACAACCTA ACACTTTGGACATCAGACAGTGCAGGAGAAGAATGTG ATGCGGCAGAAGGGGCTGAAAAC G17675. 55240817 65110599 InFrame 8297 ATGGAGGAAGACGGCGTCCGCAAGTGTAAGAAGTGC TCGA-19- GAAGGGCCTTGCCGCAAAGTGTGTAACGGAATAGGTA 2624- TTGGTGAATTTAAAGACTCACTCTCCATAAATGCTACG 01A-01R- AATATTAAACACTTCAAAAACTGCACCTCCATCAGTGG 1850- CGATCTCCACATCCTGCCGGTGGCATTTAGGGGTGACT 01.2 CCTTCACACATACTCCTCCTCTGGATCCACAGGAACTG GATATTCTGAAAACCGTAAAGGAAATCACAGGGTTTTT GCTGATTCAGGCTTGGCCTGAAAACAGGACGGACCTC CATGCCTTTGAGAACCTAGAAATCATACGCGGCAGGA CCAAGCAACAGGACCAGACAACTGTATCCAGTGTGCC CACTACATTGACGGCCCCCACTGCGTCAAGACCTGCCC GGCAGGAGTCATGGGAGAAAACAACACCCTGGTCTGG AAGTACGCAGACGCCGGCCATGTGTGCCACCTGTGCC ATCCAAACTGCACCTACGGATGCACTGGGCCAGGTCTT GAAGGCTGTCCAACGAATGGGCCTAAGATCCCGTCCA TCGCCACTGGGATGGTGGGGGCCCTCCTCTTGCTGCTG GTGGTGGCCCTGGGGATCGGCCTCTTCATGCGAAGGC GCCACATCGTTCGGAAGCGCACGCTGCGGAGGCTGCT GCAGGAGAGGGAG|ATACAGGTTTGACCCCCGTCTCA TGTTCAGCAATCGCGGCAGTGTCAGGACTCGAAGATTT TCCAAACATCTTCTG G17796. 58166911 58163739 InFrame 8298 ATGGCGGACCCCGGCCCAGATCCCGAATCTGAGTCGG TCGA-41- AATCGGTGTTCCCGCGGGAGGTCGGGCTCTTTGCAGA 5651- CTCTTACTCGGAGAAGAGCCAGTTCTGTTTCTGTGGGC 01A-01R- ATGTGCTGACCATCACGCAGAACTTTGGGTCCCGCCTC 1850- GGGGTGGCGGCGCGCGTGTGGGACGCGGCCCTGAGC 01.4 CTGTGCAATTATTTCGAGAGTCAAAATGTGGATTTCCG AGGCAAGAAGGTGATCGAACTGGGTGCGGGGACAGG CATCGTGGGGATCTTGGCAGCGCTGCAGG|TGGAACT GTCACCGCTGTTCCCAGACACACTTATTCTGGGTCTGG AGATCCGGGTGAAGGTCTCAGACTATGTACAAGACCG GATTCGGGCCCTACGCGCAGCTCCTGCAGGTGGCTTCC AGAACATCGCCTGTCTCCGTAGCAATGCCATGAAGCAC CTTCCTAACTTCTTCTACAAGGGCCAGCTGACAAAGAT GTTCTTCCTCTTCCCCGACCCACATTTCAAGCGGACAAA GCACAAGTGGCGAATCATCAGTCCCACCCTGCTAGCA GAATATGCCTACGTGCTAAGAGTTGGGGGGCTGGTGT ATACCATAACCGATGTGCTGGAGCTACACGACTGGAT GTGCACTCATTTCGAAGAGCACCCACTGTTTGAGCGTG TGCCTCTGGAGGACCTGAGTGAAGACCCCGTTGTGGG ACATCTAGGCACCTCAACTGAGGAGGGGAAGAAAGTT CTACGTAATGGAGGGAAGAATTTCCCAGCCATCTTCCG AAGAATACAAGATCCCGTCCTCCAGGCAGTGACCTCCC AAACCAGCCTGCCTGGTCAC G17666. 134210220 219103387 InFrame 8299 ATGGTCCCGGCTGCCGGTCGACGACCGCCCCGCGTCA TCGA-06- TGCGGCTCCTCGGCTGGTGGCAAGTATTGCTGTGGGT 5415- GCTGGGACTTCCCGTCCGCGGCGTGGAGG|GATACAA 01A-01R- TGTCTCTTTGCTATATGACCTTGAAAATCTTCCGGCATC 1849- CAAGGATTCCATTGTGCATCAAGCTGGCATGTTGAAGC 01.2 GAAATTGTTTTGCCTCTGTCTTTGAAAAATACTTCCAAT TCCAAGAAGAGGGCAAGGAAGGAGAGAACAGGGCAG TTATCCATTATAGGGATGATGAGACCATGTATGTTGAG TCTAAAAAGGACAGAGTCACAGTAGTCTTCAGCACAG TGTTTAAGGATGACGACGATGTGGTCATTGGAAAGGT GTTCATGCAGGAGTTCAAAGAAGGACGCAGAGCCAGC CACACAGCCCCACAGGTCCTCTTTAGCCACAGGGAACC TCCTCTGGAGCTGAAAGACACAGACGCCGCTGTGGGT GACAACATTGGCTACATTACCTTTGTGCTGTTCCCTCGT CACACCAATGCCAGTGCTCGAGACAACACCATCAACCT GATCCACACGTTCCGGGACTACCTGCACTACCACATCA AGTGCTCTAAGGCCTATATTCACACACGTATGCGGGCG AAAACGTCTGACTTCCTCAAGGTGCTGAACCGCGCACG CCCAGATGCCGAGAAAAAAGAAATGAAAACAATCACG GGGAAGACGTTTTCATCCCGC G17219. 42396776 41420897 InFrame 8300 ATGGACGGTTTCGCCGGCAGTCTCG|GTACACTTCATG TCGA-06- TTGGTGATGAAATTCGAGAAATCAATGGCATCAGTGT 0158- GGCTAACCAAACAGTGGAACAACTGCAAAAAATGCTT 01A-01R- AGGGAAATGCGGGGGAGTATTACCTTCAAGATTGTGC 1849- CAAGTTACCGCACTCAGTCTTCGTCCTGTGAGAGAGAT 01.2 TCCCCTTCCACTTCCAGACAGTCCCCAGCTAATGGTCAT AGCAGCACTAACAATTCTGTTTCGGACTTGCCATCAAC TACCCAACCAAAAGGACGACAGATCTATGTAAGAGCA CAATTTGAATATGATCCAGCCAAGGATGACCTCATCCC CTGTAAAGAAGCTGGCATTCGATTCAGAGTTGGTGAC ATCATCCAGATTATTAGTAAGGATGATCATAATTGGTG GCAGGGTAAACTGGAAAACTCCAAAAATGGAACTGCA GGTCTCATTCCTTCTCCTGAACTTCAGGAATGGCGAGT AGCTTGCATTGCCATGGAGAAGACCAAACAGGAGCAG CAGGCCAGCTGTACTTGGTTTGGCAAGAAAAAGAAGC AGTACAAAGATAAATATTTGGCAAAGCACAATGCAGT GTTTGATCAATTAGATCTTGTCACATATGAAGAAGTAG TAAAACTGCCAGCATTCAAGAGGAAAACACTAGTCTTA TTAGGCGCACATGGTGTTGGGAGAAGACACATAAAAA ACACTCTCATCACAAAGCACCCAGACCGGTTTGCGTAC CCTATTCCACATACAACCAGACCTCCAAAGAAAGACGA AGAAAATGGAAAGAATTATTACTTTGTATCTCATGACC AAATGATGCAAGACATCTCTAATAACGAGTACTTGGA GTACGGCAGCCACGAGGATGCGATGTATGGGACAAA ACTGGAGACCATCCGGAAGATCCACGAGCAGGGGCTG ATTGCAATACTGGACGTGGAGCCTCAGGCACTGAAGG TCCTGAGAACTGCAGAGTTTGCTCCTTTTGTTGTTTTCA TTGCTGCACCAACTATTACTCCAGGTTTAAATGAGGAT GAATCTCTTCAGCGTCTGCAGAAGGAGTCTGACATCTT ACAGAGAACATATGCACACTACTTCGATCTCACAATTA TCAACAATGAAATTGATGAGACAATCAGACATCTGGA GGAAGCTGTTGAGCTCGTGTGCACAGCCCCACAGTGG GTCCCTGTCTCCTGGGTCTAT G17790. 122150870 58193703 InFrame 8301 ATGTCCGGGCAGCTGGAGCGTTGCGAGCGCGAATGGC TCGA-06- ACGAGCTGGAGGGAGAATTTCAAGAACTGCAG|G ACA 5856- TGAAGAATGCAACCCTCTCCCTGAATTCTAATGACAGT 01A-01R- GAGCCAAAATATTACCCTATAGCAGTTCTGTTGAAAAA 1849- CCAGAATCAGGAGCTGCCTGAGGATGTAAACCCTGCC 01.4 AAAAAGGAGAATTACCTCTCTGAACAGGACTTTGTGTC TGTGTTTGGCATCACAAGAGGGCAATTTGCAGCTCTGC CTGGCTGGAAACAGCTCCAAATGAAGAAAGAAAAGG GGCTTTTC NYU_B 19746155 19433460 InFrame 8302 ATGGGTGGCCCACAGGACAAGGATGAACGCACAATCG CCCTTGTGAGGCCGTGGCCTTGGGGGCACCAGGCCCT GGATCCAGCATATGGCCTGGACACGATGCACCCAAGC AGGCGCAGCCTCCCCTTCCCTCTGAACTGTCAGCTTGC AAGGGTTGGAACTGCTGATTATGGAAGTCCCTCGGAT CAGAGTGATCAGCAGCTGGACTGTGCCTTGGACCTAA TGAGGCGCCTGCCTCCCCAGCAAATCGAGAAAAACCT CAGCGACCTGATCGACCTG|GATGTCCCCGTTGAGGCC CTCACCACGGTGAAGCCATACTGCAATGAGATCCATGC CCAGGCTCAACTGTGGCTCAAGAGAGACCCCAAGGCA TCCTATGATGCCTGGAAGAAGTGTCTTCCTATCAGAGG GATAGATGGCAATGGGAAAGCCCCCAGCAAATCAGAG CTCCGCCATCTCTATTTGACTGAGAAGTATGTGTGGAG GTGGAAACAGTTCCTGAGTCGTCGGGGGAAGAGGAC CTCCCCCTTGGATCTCAAACTGGGGCATAACAACTGGC TGCGACAAGTGCTTTTCACTCCAGCAACGCAGGCCGCA CGGCAGGCAGCCTGTACCATTGTGGAAGCTCTAGCCA CCATTCCCAGCCGCAAGCAGCAGGTCCTGGACCTGCTT ACCAGTTACCTGGATGAGCTGAGCATAGCTGGGGAGT GTGCAGCTGAGTACCTGGCTCTCTACCAGAAGCTCATC ACTTCTGCGCACTGGAAAGTCTACTTGGCAGCTCGGG GAGTCCTACCCTATGTGGGCAACCTCATCACCAAGGAA ATAGCTCGTCTGCTGGCCCTGGAGGAGGCTACCCTGA GTACCGATCTGCAGCAGGGTTATGCCCTTAAAAGTCTC ACAGGCCTTCTCTCCTCCTTTGTTGAGGTGGAATCCATC AAAAGACATTTTAAAAGTCGCTTGGTGGGTACTGTGCT GAATGGATACCTGTGCTTGCGGAAGCTGGTGGTGCAG AGGACCAAGCTGATCGATGAGACGCAGGACATGCTGC TGGAGATGCTGGAGGACATGACCACAGGTACAGAATC AGAAACCAAGGCCTTCATGGCTGTGTGCATTGAGACA GCCAAGCGCTACAATCTGGATGACTACCGGACCCCGG TGTTCATCTTCGAGAGGCTCTGCAGCATCATTTATCCTG AGGAGAATGAAGTCACTGAGTTCTTTGTGACCCTGGA GAAGGATCCCCAACAAGAAGACTTCTTACAGGGCAGG ATGCCTGGGAACCCGTATAGCAGCAATGAGCCAGGCA TCGGGCCGCTGATGAGGGATATAAAGAACAAGATTTG CCAGGACTGTGACTTAGTGGCCCTCCTGGAAGATGAC AGTGGCATGGAGCTTCTAGTGAACAATAAAATCATTA GTTTGGACCTTCCTGTGGCTGAAGTTTACAAGAAAGTC TGGTGTACCACGAATGAGGGAGAGCCCATGAGGATTG TTTATCGTATGCGGGGGCTGCTGGGCGATGCCACAGA GGAGTTCATTGAGTCCCTGGACTCTACTACAGatgaaga agaagatgaagaagaagTGTATAAAATGGCTGGTGTGATG GCCCAGTGTGGGGGCCTGGAATGCATGCTTAACAGAC TCGCAGGGATCAGAGATTTCAAGCAGGGACGCCACCT TCTAACAGTGCTACTGAAATTGTTCAGTTACTGCGTGA AGGTGAAAGTCAACCGGCAGCAACTGGTCAAACTGGA AATGAACACCTTGAACGTCATGCTGGGGACCCTAAACC TGGCCCTTGTAGCTGAACAAGAAAGCAAGGACAGTGG GGGTGCAGCTGTGGCTGAGCAGGTGCTTAGCATCATG GAGATCATTCTAGATGAGTCCAATGCTGAGCCCCTGAG TGAGGACAAGGGCAACCTCCTCCTGACAGGTGACAAG GATCAACTGGTGATGCTCTTGGACCAGATCAACAGCAC CTTTGTTCGCTCCAACCCCAGTGTGCTCCAGGGCCTGC TTCGCATCATCCCGTACCTTTCCTTTGGAGAGGTGGAG AAAATGCAGATCTTGGTGGAGCGATTCAAACCATACT GCAACTTTGATAAATATGATGAAGATCACAGTGGTGAT GATAAAGTCTTCCTGGACTGCTTCTGTAAAATAGCTGC TGGCATCAAGAACAACAGCAATGGGCACCAGCTGAAG GATCTGATTCTCCAGAAGGGGATCACCCAGAATGCACT TGACTACATGAAAAAGCACATCCCTAGCGCCAAGAATT TGGATGCCGACATCTGGAAAAAGTTTTTGTCTCGCCCA GCCTTGCCATTTATCCTAAGGCTGCTTCGGGGCCTGGC CATCCAGCACCCTGGCACCCAGGTTCTGATTGGAACTG ATTCCATCCCGAACCTGCATAAGCTGGAGCAGGTGTCC AGTGATGAGGGCATTGGGACCTTGGCAGAGAACCTGC TGGAAGCCCTGCGGGAACACCCTGACGTAAACAAGAA GATTGACGCAGCCCGCAGGGAGACCCGGGCAGAGAA GAAGCGCATGGCCATGGCAATGAGGCAGAAGGCCCT GGGCACCCTGGGCATGACGACAAATGAAAAGGGCCA GGTCGTGACCAAGACAGCACTCCTGAAGCAGATGGAA GAGCTGATCGAGGAGCCTGGCCTCACGTGCTGCATCT GCAGGGAGGGATACAAGTTCCAGCCCACAAAGGTCCT GGGCATTTATACCTTCACGAAGCGGGTAGCCTTGGAG GAGATGGAGAATAAGCCCCGGAAACAGCAGGGCTAC AGCACCGTGTCCCACTTCAACATTGTGCACTACGACTG CCATCTGGCTGCCGTCAGGTTGGCTCGAGGCCGGGAA GAGTGGGAGAGTGCCGCCCTGCAGAATGCCAACACCA AGTGCAACGGGCTCCTTCCGGTCTGGGGACCTCATGTC CCTGAATCAGCTTTTGCCACTTGCTTGGCAAGACACAA CACTTACCTCCAGGAATGTACAGGCCAGCGGGAGCCC ACGTATCAGCTCAACATCCATGACATCAAACTGCTCTTC CTGCGCTTCGCCATGGAGCAGTCGTTCAGCGCAGACA CTGGCGGGGGCGGCCGGGAGAGCAACATCCACCTGA TCCCGTACATCATTCACACTGTGCTTTACGTCCTGAACA CAACCCGAGCAACTTCCCGAGAAGAGAAGAACCTCCA AGGCTTTCTGGAACAGCCCAAGGAGAAGTGGGTGGA GAGTGCCTTTGAAGTGGACGGGCCCTACTATTTCACAG TCTTGGCCCTTCACATCCTGCCCCCTGAGCAGTGGAGA GCCACACGTGTGGAAATCTTGCGGAGGCTGTTGGTGA CCTCGCAGGCTCGGGCAGTGGCTCCAGGTGGAGCCAC CAGGCTGACAGATAAGGCAGTGAAGGACTATTCCGCT TACCGTTCTTCCCTTCTCTTTTGGGCCCTCGTCGATCTC ATTTACAACATGTTTAAGAAACAAACAACCCCAACTGT GGGAGGGATTGACACTGGCAGCCTGGAGCCTTGTGTC TGTGAGAAGGTGCCTACCAGTAACACAGAGGGAGGCT GGTCCTGCTCTCTCGCTGAGTACATCCGCCACAACGAC ATGCCCATCTACGAAGCTGCCGACAAAGCCCTGAAAA CCTTCCAGGAGGAGTTCATGCCAGTGGAGACCTTCTCA GAGTTCCTCGATGTGGCCGGTCTTTTATCAGAAATCAC CGATCCAGAGAGCTTCCTGAAGGACCTGTTGAACTCA GTCCCC G17657. 100438902 100348442 InFrame 8303 ATGAACGGACAGTTGGATCTAAGTGGGAAGCTAATCA TCGA-19- TCAAAGCTCAACTTGGGGAGGATATTCGGCGAATTCCT 1787- ATTCATAATGAAGATATTACTTATGATGAATTAGTGCT 01B-01R- AATGATGCAACGAGTTTTCAGAGGAAAACTTCTGAGT 1850- AATGATGAAGTAACAATAAAGTATAAAGATGAAGATG 01.2 GAGATCTTATAACAATTTTTGATAGTTCTGACCTTTCCT TTGCAATTCAGTGCAGTAGGATACTGAAACTGACATTA TTTG|GAAAATCTACTTCCTCATCAAGCACCCCTACAGA GTTCTGCAGGAATGGTGGAACCTGGGAAAATGGCAGA TGTATTTGTACAGAAGAGTGGAAAGGACTGAGATGTA CAATTGCTAATTTTTGTGAAAATAGTACCTATATGGGTT TTACTTTTGCCAGAATCCCAGTGGGCAGATATGGACCA TCCTTGCAAACATGTGGCAAGGATACTCCAAATGCGG GCAATCCAATGGCAGTCCGGTTGTGCAGTCTCTCTCTA TATGGAGAGATAGAATTACAAAAAGTGACAATAGGAA ATTGCAATGAAAATCTGGAAACCCTGGAAAAGCAGGT AAAGGATGTCACAGCACCACTTAATAACATTTCTTCTG AAGTCCAGATTTTAACATCTGATGCCAATAAATTAACT GCTGAGAACATCACTAGTGCTACGCGAGTGGTTGGAC AGATATTCAACACTTCCAGAAATGCTTCACCTGAGGCA AAGAAAGTTGCCATAGTAACAGTGAGTCAACTCCTAG ATGCCAGTGAAGATGCTTTTCAAAGAGTTGCTGCTACT GCTAATGATGATGCCCTTACAACGCTTATTGAGCAAAT GGAGACTTATTCCTTGTCTTTGGGTAATCAATCAGTGG TGGAACCTAACATAGCAATACAGTCAGCAAATUCTCT TCAGAAAATGCGGTGGGGCCTTCAAATGTTCGCTTCTC TGTGCAGAAAGGAGCTAGCAGTTCTCTAGTTTCTAGTT CAACATTTATACATACAAATGTGGATGGCCTTAACCCA GATGCACAGACTGAGCTTCAGGTCTTGCTTAATATGAC GAAAAATTACACCAAGACATGCGGCTTTGTAGTTTATC AAAATGACAAGCTTTTCCAATCAAAAACTTTTACAGCT AAATCGGATTTTAGTCAAAAAATTATCTCAAGCAAAAC TGATGAAAATGAGCAAGATCAGAGTGCTTCTGTTGAC ATGGTCTTTAGTCCAAAGTACAACCAAAAAGAATTTCA ACTCTATTCCTATGCCTGTGTCTATTGGAATTTGTCAGC GAAGGACTGGGACACATATGGCTGTCAAAAAGACAAG GGCACTGATGGATTCCTGCGCTGCCGCTGCAACCATAC TACTAATTTTGCTGTATTAATGACTTTCAAAAAGGATTA TCAATATCCCAAATCACTTGACATATTATCCAACGTTGG ATGTGCACTGTCTGTTACTGGTCTGGCTCTCACAGTTAT ATTTCAGATTGTCACCAGGAAAGTCAGAAAAACCTCAG TAACCTGGGTTTTGGTCAATCTGTGCATATCAATGTTG ATTTTCAACCTCCTCTTTGTGTTTGGAATTGAAAACTCC AATAAGAACTTGCAGACAAGTGATGGTGACATCAATA ATATTGACTTTGACAATAATGACATACCCAGGACAGAC ACCATTAACATCCCGAATCCCATGTGCACTGCGATTGC CGCCTTACTGCACTATTTTCTGTTAGTGACATTTACCTG GAACGCACTCAGCGCTGCACAGCTCTATTACCTTCTAA TAAGGACCATGAAGCCTCTTCCTCGGCATTTCATTCTTT TCATCTCATTAATTGGATGGGGAGTCCCAGCTATAGTA GTGGCTATAACAGTGGGAGTTATTTATTCTCAGAATGG AAATAATCCACAGTGGGAATTAGACTACCGGCAAGAG AAAATCTGCTGGCTGGCAATTCCAGAACCCAATGGTGT TATAAAAAGTCCGCTGTTGTGGTCATTCATCGTACCTG TAACCATTATCCTCATCAGCAATGTTGTTATGTTTATTA CAATCTCGATCAAAGTGCTGTGGAAGAATAACCAGAA CCTGACAAGCACAAAAAAAGTTTCATCCATGAAGAAG ATTGTTAGCACATTATCTGTTGCAGTTGTTTTTGGAATT ACCTGGATTCTAGCATACCTGATGCTAGTTAATGATGA TAGCATCAGGATCGTCTTCAGCTACATATTCTGCCTTTT CAACACTACACAGGGATTGCAAATTTTTATCCTGTACA CTGTTAGAACAAAAGTCTTCCAGAGTGAAGCTTCCAAA GTGTTGATGTTGCTATCGTCTATTGGGAGAAGGAAGTC ATTGCCTTCAGTGACGCGGCCGAGGCTGCGTGTAAAG ATGTATAATTTCCTCAGGTCATTGCCAACCTTACATGAA CGCTTTAGGCTACTGGAAACCTCTCCGAGTACTGAGGA AATCACACTCTCTGAAAGTGACAATGCAAAGGAAAGC ATC G17643. 43976965 52740660 InFrame 8304 ATGGCCCCCGCCCGTCTGTTCGCGCTGCTGCTGTTCTTC TCGA-12- GTAGGCGGAGTCGCCGAGTCG|GATTACAAGGGCCAG 5295- AAGCTAGCTGAACAGATGTTTCAGGGAATTATTCTTTT 01A-01R- TTCTGCAATAGTTGGATTTATCTACGGGTACGTGGCTG 1849- AACAGTTCGGGTGGACTGTCTATATAGTTATGGCCGG 01.2 ATTTGCTTTTTCATGTTTGCTGACACTTCCTCCATGGCC CATCTATCGCCGGCATCCTCTCAAGTGGTTACCTGTTCA AGAATCAAGCACAGACGACAAGAAACCAGGGGAAAG AAAAATTAAGAGGCATGCTAAAAATAAT NYU_G 100191807 102260661 InFrame 8305 ATGCGCTCCATTAGGAAGAGGTGGACGATCTGCACAA TAAGTCTGCTCCTGATCTTTTATAAGACAAAAGAAATA GCAAGAACTGAGGAGCACCAGGAGACGCAACTCATCG GAGATGGTGAATTGTCTTTGAGTCGGTCACTTGTCAAT AGCTCTGATAAAATCATTCGAAAGGCTGGCTCTTCAAT CTTCCAGCACAATGTAGAAGGTTGGAAAATCAATTCCT CTTTGGTCCTAGAGATAAGGAAGAACATACTTCGTTTC TTAGATGCAGAACGAGATGTGTCAGTGGTCAAGAGCA GTTTTAAGCCTGGTGATGTCATACACTATGTGCTTGAC AGGCGCCGGACACTAAACATTTCTCATGATCTACATAG CCTCCTACCTGAAGTTTCACCAATGAAGAATCGCAGGT TTAAGACCTGTGCAGTTGTTGGAAATTCTGGCATTCTG TTAGACAGTGAATGTGGAAAGGAGATTGACAGTCACA ATTTTGTAATAAGGTGTAATCTAGCTCCTGTGGTGGAG TTTGCTGCAGATGTGGGAACTAAATCAGATTTTATTAC CATGAATCCATCAGTTGTACAAAGAGCATTTGGAGGCT TTCGAAATGAGAGTGACAGAGAAAAATTTGTGCATAG ACTTTCCATGCTGAATGACAGTGTCCTTTGGATTCCTGC TTTCATGGTCAAAGGAGGAGAGAAGCACGTGGAGTG GGTTAATGCATTAATCCTTAAGAATAAACTGAAAGTGC GAACTGCCTATCCGTCATTGAGACTTATTCATGCTGTCA GAGG|GTTTTGTGATGAAGGAACCTGTACAGATAAAG CCAATATTCTGTATGCCTGGGCGAGAAATGCTCCCCCT ACCCGGCTCCCCAAAGGTGTTGGATTCAGAGTTGGAG GAGAGACTGGAAGTAAATACTTTGTACTACAGGTACA CTATGGGGATATTAGTGCTTTTAGAGATAATAACAAGG ACTGTTCTGGTGTGTCCTTACACCTCACACGTCTGCCAC AGCCTTTAATTGCTGGCATGTACCTTATGATGTCTGTTG ACACTGTTATCCCAGCAGGAGAAAAAGTGGTGAATTC TGACATTTCATGCCATTATAAAAATTATCCAATGCATGT CTTTGCCTATAGAGTTCACACTCACCATTTAGGTAAGG TAGTAAGTGGATACAGAGTAAGAAATGGACAGTGGAC ACTGATTGGACGGCAGAGCCCTCAGCTGCCACAGGCT TTCTACCCTGTGGGGCATCCAGTTGATGTAAGTTTTGG TGACCTACTGGCTGCAAGATGTGTATTCACTGGTGAAG GAAGGACAGAAGCCACACACATTGGTGGCACGTCTAG TGATGAAATGTGCAACTTATACATTATGTATTACATGG AAGCCAAGCATGCAGTTTCTTTCATGACCTGTACCCAG AATGTAGCTCCAGATATGTTCAGAACCATACCACCAGA GGCCAACATTCCAATTCCCGTGAAGTCTGATATGGTTA TGATGCATGAACATCATAAAGAAACAGAATATAAAGA TAAGATTCCTTTACTACAGCAGCCAAAACGAGAAGAA GAAGAAGTGTTAGACCAGGGTGATTTCTATTCACTACT TTCCAAGCTGCTAGGAGAAAGGGAAGATGTTGTTCAT GTGCACAAATATAATCCTACAGAAAAGGCAGAATCAG AGTCAGACCTGGTAGCTGAGATTGCAAATGTAGTCCA AAAAAAGGATCTTGGTCGATCTGATGCCAGAGAGGGT GCAGAACATGAGAGGGGTAATGCTATTCTTGTCAGAG ACAGAATTCACAAATTCCACAGACTAGTATCTACCTTG AGGCCACCAGAGAGCAGAGTTTTCTCATTACAGCAGC CCCCACCTGGTGAAGGCACCTGGGAACCAGAACACAC AGGAGATTTCCACATGGAAGAGGCACTGGATTGGCCT GGAGTATACTTGTTACCAGGCCAGGTTTCTGGGGTGG CTCTAGACCCTAAGAATAACCTGGTGATTTTCCACAGA GGTGACCATGTCTGGGATGGAAACTCGTTTGACAGCA AGTTTGTTTACCAGCAAATAGGACTCGGACCAATTGAA GAAGACACTATTCTTGTCATAGATCCAAATAATGCTGC AGTACTCCAGTCCAGTGGAAAAAATCTGTTTTACTTGC CACATGGCTTGAGTATAGATAAAGATGGGAATTATTG GGTCACAGACGTGGCTCTCCATCAGGTGTTCAAACTGG ATCCAAACAATAAAGAAGGCCCTGTATTAATCCTGGGA AGGAGCATGCAACCAGGCAGTGACCAGAATCACTTCT GTCAACCCACTGATGTGGCTGTGGATCCAGGCACTGG AGCCATTTATGTATCAGATGGTTACTGCAACAGCAGGA TTGTGCAGTTTTCACCAAGTGGAAAGTTCATCACACAG TGGGGAGAAGAGTCTTCAGGGAGCAGTCCTCTGCCAG GCCAGTTCACTGTTCCTCACAGCTTGGCTCTTGTGCCTC TTTTGGGCCAATTATGTGTGGCAGACCGGGAAAATGG TCGGATCCAGTGTTTTAAAACTGACACCAAAGAATTTG TGAGAGAGATTAAGCATTCATCATTTGGAAGAAATGT ATTTGCAATTTCATATATACCAGGCTTGCTCTTTGCAGT GAATGGGAAGCCTCATTTTGGGGACCAAGAACCTGTA CAAGGATTTGTGATGAACTTTTCCAATGGGGAAATTAT AGACATCTTCAAGCCAGTGCGCAAGCACTTTGATATGC CTCATGATATTGTTGCATCTGAAGATGGGACTGTGTAC ATTGGAGATGCTCATACCAACACCGTGTGGAAGTTCAC CTTGACTGAGAAATTGGAACATCGATCAGTTAAAAAG GCTGGCATTGAGGTCCAGGAAATCAAAGAAGCCGAG GCAGTTGTTGAAACCAAAATGGAGAACAAACCCACCT CCTCAGAATTGCAGAAGATGCAAGAGAAACAGAAACT GATCAAAGAGCCAGGCTCGGGAGTGCCTGTTGTTCTC ATTACAACCCTTCTGGTTATTCCGGTGGTTGTCCTGCTG GCCATTGCCATATTTATTCGGTGGAAAAAATCAAGGGC CTTTGGAGCAGATTCTGAACACAAACTCGAGACGAGTT CAGGAAGAGTACTGGGAAGATTTAGAGGAAAGGGAA GTGGAGGCTTAAACCTTGGTAATTTCTTTGCAAGCCGT AAGGGCTACAGTCGAAAAGGGTTTGACCGGCTTAGCA CTGAGGGCAGTGACCAAGAGAAAGAGGATGATGGAA GTGAATCAGAAGAGGAGTATTCAGCACCTCTGCCTGC GCTCGCACCTTCCTCCTCC G17494. 48965246 48265844 InFrame 8306 ATGTCAGTGGACATGAATAGCCAGGGGTCTGACAGCA TCGA-14- ATGAAGAGGACTATGACCCAAATTGTgaggaagaggaaga 2554- agaagaagaagaCGACCCTGGGGACATAGAGGACTATTA 01A-01R- CGTGGGAGTAGCCAGCGATGTGGAGCAGCAGGGGGC 1850- TGATGCCTTTGATCCCGAGGAGTACCAGTTCACTTGCT 01.2 TGACCTACAAGGAATCTGAGGGTGCCCTCAATGAGCA CATGACCAGCTTAGCTTCTGTCCTAAAG|GATGGGGAC CCAGACACGCCAAAGCCTGTGAGCTTCACAGTGAAGG AGACAGTGTGCCCCAGGACGACACAGCAGTCACCAGA GGATTGTGACTTCAAGAAGGACGGGCTGGTGAAGCG GTGTATGGGGACAGTGACCCTCAACCAGGCCAGGGGC TCCTTTGACATCAGTTGTGATAAGGATAACAAGAGATT TGCCCTGCTGGGTGATTTCTTCCGGAAATCTAAAGAGA AGATTGGCAAAGAGTTTAAAAGAATTGTCCAGAGAAT CAAGGATTTTTTGCGGAATCTTGTACCCAGGACAGAGT CC G17196. 58123422 94827533 InFrame 8307 ATGAGCCGGGGCGCGGGCGCGCTTCAGCGCCGGACA TCGA-06- ACGACCTACCTCATCTCGCTGACCCTGGTTAAGCTCGA 0178- gtcggtgcctccgccgccgccttctccgtctgcggccgcggccggcgcc 01A-01R- gccggtgccAGAGGCTCCGAGACTGGGGATCCTGGCAGC 1849- CCCCGAGGCGCGGAGGAGCCGGGCAAGAAGCGGCAC 01.2 GAACGTCTCTTCCACCGGCAGGATGCGCTGTGGATCA GCACGAGCAGCGCGGGCACCGGGGGCGCGGAGCCCC CAGCCCTGTCCCCGGCTCCGGCCAGTCCGGCCCGCCCA GTCTCCCCCGCTCCCGGCCGCCGCCTCTCCCTCTGGGC CGTCCCTCCGGGACCCCCGCTCTCCGGGGGACTGAGC CCCGACCCCAAGCCTGGGGGCGCCCCCACCTCCTCCCG GCGCCCCCTGCTCAGCAGCCCGAGCTGGGGCGGCCCG GAGCCCGAAGGCCGGGCGGGCGGCGGCATCCCTGGC TCATCCTCTCCGCACCCTGGCACCGGCAGCCGGAGGCT CAAGGTGGCGCCTCCTCCGCCGGCTCCCAAGCCTTGCA AGACCGTGACCACGAGTGGAGCCAAAGCCGGCGGGG GCAAGGGCGCGGGTAGCCGCCTGTCATGGCCCGAAA GCGAGGGCAAGCCCAGGGTCAAGGGGTCAAAGAGCA GCGCCGGGACTGGAGCTTCGGTCTCTgccgccgccaccgcc gccgccgccgGGGGAGGGGGCTCTACAGCTTCGACCTCT GGTGGGGTCGGGGCTGGGGCTGGAGCCCGAGGGAA GTTGTCCCCTCGGAAAGGCAAGAGTAAGACCTTGGAC AACAGTGACTTGCATCCGGGACCGCCTGCCGGCTCTCC TCCTCCGCTAACCCTCCCACCAACTCCGAGTCCAGCCAC TGCTGTCACCGCTGCTTCCGCGCAGCCCCCCGGGCCTG CACCTCCAATCACTCTGGAGCCTCCAGCTCCGGGGCTG AAACGGGGCCGGGAGGGGGGCCGAGCATCCACTCGT GACCGCAAGATGCTCAAGTTTATCAGCGGCATCTTCAC CAAGAGCACAGGAGGGCCTCCTGGCTCCGGGCCCCTT CCCGGACCCCCCAGCCTGTCTTCTGGCAGCGGGTCCAG GGAGCTGCTGGGCGCCGAGCTCCGCGCTTCCCCTAAG GCTGTGATCAATAGCCAGGAATGGACTTTGAGCCGCT CCATTCCTGAACTGCGCCTGGGTGTGCTGGGCGATGCC AGGAGTGGGAAGTCATCGCTCATCCACCGATTCCTGAC TGGCTCATACCAGGTGCTGGAGAAGACAGAGAGTGA GCAGTACAAGAAAGAAATGTTGGTGGATGGACAGAC ACATCTGGTGCTAATCCGAGAGGAAGCTGGGGCACCT GATGCCAAGTTCTCAGGCTGGGCAGATGCTGTGATCTT CGTCTTCAGCCTGGAGGATGAGAACAGTTTCCAGGCT GTGAGCCGTCTCCATGGGCAGCTGAGTTCCCTTCGCGG GGAGGGACGAGGAGGCCTGGCCTTGGCACTGGTGGG GACACAAGACAGGATCAGTGCTTCCTCCCCTCGGGTG GTGGGAGATGCTCGTGCCAGAGCTCTGTGCGCGGACA TGAAACGCTGCAGCTACTATGAGACTTGTGCAACCTAT GGGCTCAATGTGGATCGGGTCTTCCAGGAGGTGGCCC AGAAGGTGGTGACCTTGCGCAAGCAGCAACAGCTTCT GGCTGCCTGCAAGTCCCTGCCCAGCTCCCCAAGCCACT CAGCTGCATCCACTCCGGTAGCTGGCCAGGCTAGTAAC GGGGGCCACACTAGCGACTACTCTTCTTCCCTCCCGTC CTCACCGAATGTTGGTCACCGGGAGCTCCGAGCCGAG GCAGCTGCAGTGGCTGGATTGAGCACCCCAGGGTCCC TGCACCGGGCAGCCAAGCGCAGGACCAGCCTTTTTGC GAATCGTCGGGGTAGTGACTCCGAGAAACGAAGCTTG GATAGTCGGGGAGAGACAACAGGGAGTGGGCGAGCC ATCCCCATCAAACAGAGCTTCCTACTAAAACGAAGTGG CAATTCCTTGAACAAAGAATGGAAGAAGAAATATGTA ACCCTGTCCAGTAATGGCTTTCTACTCTACCACCCCAGT ATTAACGATTACATCCACAGTACCCACGGCAAGGAGAT GGACTTGCTGCGAACAACAGTCAAAGTCCCGGGCAAG CGGCCCCCGAGGGCCATCTCTGCCTTTGGCCCCTCAGC CAGCATTAACGGGCTCGTCAAGGACATGAGCACTGTC CAGATGGGTGAAGGCCTGGAAGCCACTACTCCCATGC CAAGCCCTAGCCCCAGCCCCAGTTCCCTGCAGCCACCA CCAGATCAGACATCCAAACACCTGCTGAAGCCAGACC GGAATTTGGCCCGAGCCCTCAGCACGGACTGTACCCC ATCTGGAGACCTGAGCCCCCTGAGTCGGGAACCCCCTC CTTCTCCCATGGTGAAGAAGCAGAGGAGGAAAAAATT GACAACACCATCCAAGACTGAAGGCTCGGCTGGGCAG GCTGAAGTATGAAGGTTATTCTTTCAGCAGTGTCCTGT ATTATGGAAATGAAGCTACTCTTCTTATTTTTGATCTGC TGTTCTTCTGTGTTGTGGATTTGGCTTGCCAAAATTTTA TTTTAGCATCCTTCCTTACATATCTACAACAAGAGATTT TTAGATATATCCGTAATACAGTAGGACAAAAGAATTTG GCATCCAAAACATTGGTGGATCAAAGATTTTTGATT G17782. 95392394 9544862 InFrame 8308 ATGACCCACTTCAACAAGGGCCCTTCCTATGGGCTCTC TCGA-26- GGCCGAAGTCAAGAACAAG|GTGTTGTGTAACGGACC 5136- AGGAACATGTGTTCCTATCTGTGTATCTGCCCTTCTCCT 01B-01R- TGGGATACTAGGAATAAAGAAAGTGATCATTGTCTAC 1850- GTTGAAAGCATCTGCCGTGTAGAAACGTTATCCATGTC 01.4 CGGAAAGATTCTGTTTCATCTCTCAGATTACTTCATTGT TCAGTGGCCGGCTCTGAAAGAAAAGTATCCCAAATCG GTGTACCTTGGGCGAATTGTT GBM- 55639964 68645358 InFrame 8309 ATGAGGCGCCAGCCTGCGAAGGTGGCGGCGCTGCTGC CUMC3296_L1 TCGGGCTGCTCTTGGAG|CATATTGAAGGTGATGACCT GCATATCCAGAGGAATGTGCAAAAGCTGAAGGACACA GTGAAAAAGCTTGGAGAGAGTGGAGAGATCAAAGCA ATTGGAGAACTGGATTTGCTGTTTATGTCTCTGAGAAA TGCCTGCATT G17199. 55087058 102784508 InFrame 8310 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-06- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 0744- GGAGGAAAAGAAAG|CTGACATAGCCCAGAGATACA 01A-01R- GGATAAGCAAATACCCAACCCTCAAATTGTTTCGTAAT 1849- GGGATGATGATGAAGAGAGAATACAGGGGTCAGCGA 01.2 TCAGTGAAAGCATTGGCAGATTACATCAGGCPACAAA AAAGTGACCCCATTCAAGAAATTCGGGACTTAGCAGA AATCACCACTCTTGATCGCAGCAAAAGAAATATCATTG GATATTTTGAGCAAAAGGACTCGGACAACTATAGAGT TTTTGAACGAGTAGCGAATATTTTGCATGATGACTGTG CCTTTCTTTCTGCATTTGGGGATGTTTCAAAACCGGAA AGATATAGTGGCGACAACATAATCTACAAACCACCAG GGCATTCTGCTCCGGATATGGTGTACTTGGGAGCTATG ACAAATTTTGATGTGACTTACAATTGGATTCAAGATAA ATGTGTTCCTCTTGTCCGAGAAATAACATTTGAAAATG GAGAGGAATTGACAGAAGAAGGACTGCCTTTTCTCAT ACTCTTTCACATGAAAGAAGATACAGAAAGTTTAGAAA TATTCCAGAATGAAGTAGCTCGGCAATTAATAAGTGAA AAAGGTACAATAAACTTTTTACATGCCGATTGTGACAA ATTTAGACATCCTCTTCTGCACATACAGAAAACTCCAG CAGATTGTCCTGTAATCGCTATTGACAGCTTTAGGCAT ATGTATGTGTTTGGAGACTTCAAAGATGTATTAATTCC TGGAAAACTCAAGCAATTCGTATTTGACTTACATTCTG GAAAACTGCACAGAGAATTCCATCATGGACCTGACCC AACTGATACAGCCCCAGGAGAGCAAGCCCAAGATGTA GCAAGCAGTCCACCTGAGAGCTCCTTCCAGAAACTAGC ACCCAGTGAATATAGGTATACTCTATTGAGGGATCGA GATGAGCTT G17792. 6996029 8288288 InFrame 8311 ATGACTGATGGAAAACTCTCCACCTCTACAAATGGCGT TCGA-28- AGCCTTCATGGGTATTCTGGATGGTCGACCAGGAAAC 5204- CCCCTTCAGAACCTGCAACACGTCAATCTCAAGGCGCC 01A-01R- CCGACTCCTCTCCGCGCCTGAGTACGGGCCCAAGCTGA 1850- AACTCAGGGCTTTAGAAGACCGGCACAGCCTCCAGTC 01.4 CGTGGACTCGGGGATTCCTACCCTGGAGATCGGGAAC CCGGAGCCTGTACCCTGCAGCGCGGTCCACGTGAGGA GGAAGCAGTCCGACTCCGACCTCATCCCCGAGCGGGC CTTCCAGAGCGCCTGCGCGCTGCCATCCTGTGCGCCAC CAGCTCCTAGCAGCACCGAGCGGGAACAGAGCGTGCG CAAATCCTCCACGTTTCCCAGGACAGGCTATGACTCGG TAAAGCTCTATAGCCCGACCTCCAAAGCCCTGACCCGC AGCGATGATGTCTCCGTCTGCAGCGTGTCCAGTCTTGG GACAGAGCTGTCCACCACGCTGTCCGTCAGCAATGAG GACATCTTGGACCTTGTGGTCACGAGCAGCTCCAGTGC CATTGTGACCCTGGAGAATGACGATGACCCACAGTTTA CCAACGTCACCTTGAGCTCTATCAAGGAAACCCGTGGC TTACACCAGCAGGACTGTGTTCATGAAGCTGAGGAGG GGAGTAAATTGAAAATATTGGGGCCATTTAGTAACTTC TTTGCAAGGAACTTGCTTGCTAGAAAACAAAGTGCAA GGCTTGACAAACACAATGACTTGGGATGGAAGTTATTT GGGAAAGCGCCACTCCGAGAGAATGCCCAGAAGGATT CAAAGAGAATACAGAAGgaatatgaagacaaggctggaagac ctagCAAGCCACCCTCTCCAAAGCAGAATGTGAGGAAG AATCTTGACTTTGAACCACTTTCCACCACCGCACTCATC CTCGAGGACAGACCAGC|ACACCCGCTGTTTGGCCGCA ACGTGCCCCTGTCCAGCGGTTCTGGCTTCATCATGTCA GAGGCCGGCCTGATCATCACCAATGCCCACGTGGTGT CCAGCAACAGTGCTGCCCCGGGCAGGCAGCAGCTCAA GGTGCAGCTACAGAATGGGGACTCCTATGAGGCCACC ATCAAAGACATCGACAAGAAGTCGGACATTGCCACCA TCAAGATCCATCCCAAGAAAAAGCTCCCTGTGTTGTTG CTGGGTCACTCGGCCGACCTGCGGCCTGGGGAGTTTG TGGTGGCCATCGGCAGTCCCTTCGCCCTACAGAACACA GTGACAACGGGCATCGTCAGCACTGCCCAGCGGGAGG GCAGGGAGCTGGGCCTCCGGGACTCCGACATGGACTA CATCCAGACGGATGCCATCATCAACTACGGGAACTCCG GGGGACCACTGGTGAACCTGGATGGCGAGGTCATTGG CATCAACACGCTCAAGGTCACGGCTGGCATCTCCTTTG CCATCCCCTCAGACCGCATCACACGGTTCCTCACAGAG TTCCAAGACAAGCAGATCAAAGACTGGAAGAAGCGCT TCATCGGCATACGGATGCGGACGATCACACCAAGCCT GGTGGATGAGCTGAAGGCCAGCAACCCGGACTTCCCA GAGGTCAGCAGTGGAATTTATGTGCAAGAGGTTGCGC CGAATTCACCTTCTCAGAGAGGCGGCATCCAAGATGG TGACATCATCGTCAAGGTCAACGGGCGTCCTCTAGTGG ACTCGAGTGAGCTGCAGGAGGCCGTGCTGACCGAGTC TCCTCTCCTACTGGAGGTGCGGCGGGGGAACGACGAC CTCCTCTTCAGCATCGCACCTGAGGTGGTCATG G17476. 7310150 32328393 InFrame 8312 ATGAGACTCCTCCCCCGCTTGCTGCTGCTTCTCTTACTC TCGA-06- GTGTTCCCTGCCACTGTCTTGTTCCGAGGCGGCCCCAG 2569- AGGCTTGTTAGCAGTGGCACAAGATCTTACAGAGGAT 01A-01R- GAAGAAACAGTAGAAGATTCCATAATTGAGGATGAAG 1849- ATGATGAAGCCGAGGTAGAAGAAGATGAACCCACAG 01.2 ATTTG|CACACTGTCCGTGAAGAAACGATGATGGTGAT GACTGAAGACATGCCTTTGGAAATTTCTTATGTGCCTT CTACTTATTTGACTGAAATCACTCATGTCTCACAAGCCC TATTAGAAGTGGAACAACTTCTCAATGCTCCTGACCTC TGTGCTAAGGACTTTGAAGATCTCTTTAAGCAAGAGGA GTCTCTGAAGAATATAAAAGATAGTCTACAACAAAGCT CAGGTCGGATTGACATTATTCATAGCAAGAAGACAGC AGCATTGCAAAGTGCAACGCCTGTGGAAAGGGTGAAG CTACAGGAAGCTCTCTCCCAGCTTGATTTCCAATGGGA AAAAGTTAACAAAATGTACAAGGACCGACAAGGGCGA TTTGACAGATCTGTTGAGAAATGGCGGCGTTTTCATTA TGATATAAAGATATTTAATCAGTGGCTAACAGAAGCTG AACAGTTTCTCAGAAAGACACAAATTCCTGAGAATTGG GAACATGCTAAATACAAATGGTATCTTAAGGAACTCCA GGATGGCATTGGGCAGCGGCAAACTGTTGTCAGAACA TTGAATGCAACTGGGGAAGAAATAATTCAGCAATCCTC AAAAACAGATGCCAGTATTCTACAGGAAAAATTGGGA AGCCTGAATCTGCGGTGGCAGGAGGTCTGCAAACAGC TGTCAGACAGAAAAAAGAGGCTAGAAGAACAAAAGA ATATCTTGTCAGAATTTCAAAGAGATTTAAATGAATTT GTTTTATGGTTGGAGGAAGCAGATAACATTGCTAGTAT CCCACTTGAACCTGGAAAAGAGCAGCAACTAAAAGAA AAGCTTGAGCAAGTCAAGTTACTGGTGGAAGAGTTGC CCCTGCGCCAGGGAATTCTCAAACAATTAAATGAAACT GGAGGACCCGTGCTTGTAAGTGCTCCCATAAGCCCAG AAGAGCAAGATAAACTTGAAAATAAGCTCAAGCAGAC AAATCTCCAGTGGATAAAGGTTTCCAGAGCTTTACCTG AGAAACAAGGAGAAATTGAAGCTCAAATAAAAGACCT TGGGCAGCTTGAAAAAAAGCTTGAAGACCTTGAAGAG CAGTTAAATCATCTGCTGCTGTGGTTATCTCCTATTAGG AATCAGTTGGAAATTTATAACCAACCAAACCAAGAAG GACCATTTGACGTTAAGGAAACTGAAATAGCAGTTCA AGCTAAACAACCGGATGTGGAAGAGATTTTGTCTAAA GGGCAGCATTTGTACAAGGAAAAACCAGCCACTCAGC CAGTGAAGAGGAAGTTAGAAGATCTGAGCTCTGAGTG GAAGGCGGTAAACCGTTTACTTCAAGAGCTGAGGGCA AAGCAGCCTGACCTAGCTCCTGGACTGACCACTATTGG AGCCTCTCCTACTCAGACTGTTACTCTGGTGACACAAC CTGTGGTTACTAAGGAAACTGCCATCTCCAAACTAGAA ATGCCATCTTCCTTGATGTTGGAGGTACCTGCTCTGGC AGATTTCAACCGGGCTTGGACAGAACTTACCGACTGG CTTTCTCTGCTTGATCAAGTTATAAAATCACAGAGGGT GATGGTGGGTGACCTTGAGGATATCAACGAGATGATC ATCAAGCAGAAGGCAACAATGCAGGATTTGGAACAGA GGCGTCCCCAGTTGGAAGAACTCATTACCGCTGCCCAA AATTTGAAAAACAAGACCAGCAATCAAGAGGCTAGAA CAATCATTACGGATCGAATTGAAAGAATTCAGAATCAG TGGGATGAAGTACAAGAACACCTTCAGAACCGGAGGC AACAGTTGAATGAAATGTTAAAGGATTCAACACAATG GCTGGAAGCTAAGGAAGAAGCTGAGCAGGTCTTAGG ACAGGCCAGAGCCAAGCTTGAGTCATGGAAGGAGGG TCCCTATACAGTAGATGCAATCCAAAAGAAAATCACAG AAACCAAGCAGTTGGCCAAAGACCTCCGCCAGTGGCA GACAAATGTAGATGTGGCAAATGACTTGGCCCTGAAA CTTCTCCGGGATTATTCTGCAGATGATACCAGAAAAGT CCACATGATAACAGAGAATATCAATGCCTCTTGGAGAA GCATTCATAAAAGGGTGAGTGAGCGAGAGGCTGCTTT GGAAGAAACTCATAGATTACTGCAACAGTTCCCCCTGG ACCTGGAAAAGTTTCTTGCCTGGCTTACAGAAGCTGAA ACAACTGCCAATGTCCTACAGGATGCTACCCGTAAGGA AAGGCTCCTAGAAGACTCCAAGGGAGTAAAAGAGCTG ATGAAACAATGGCAAGACCTCCAAGGTGAAATTGAAG CTCACACAGATGTTTATCACAACCTGGATGAAAACAGC CAAAAAATCCTGAGATCCCTGGAAGGTTCCGATGATG CAGTCCTGTTACAAAGACGTTTGGATAACATGAACTTC AAGTGGAGTGAACTTCGGAAAAAGTCTCTCAACATTA GGTCCCATTTGGAAGCCAGTTCTGACCAGTGGAAGCG TCTGCACCTTTCTCTGCAGGAACTTCTGGTGTGGCTAC AGCTGAAAGATGATGAATTAAGCCGGCAGGCACCTAT TGGAGGCGACTTTCCAGCAGTTCAGAAGCAGAACGAT GTACATAGGGCCTTCAAGAGGGAATTGAAAACTAAAG AACCTGTAATCATGAGTACTCTTGAGACTGTACGAATA TTTCTGACAGAGCAGCCTTTGGAAGGACTAGAGAAAC TCTACCAGGAGCCCAGAGAGCTGCCTCCTGAGGAGAG AGCCCAGAATGTCACTCGGCTTCTACGAAAGCAGGCT GAGGAGGTCAATACTGAGTGGGAAAAATTGAACCTGC ACTCCGCTGACTGGCAGAGAAAAATAGATGAGACCCT TGAAAGACTCCGGGAACTTCAAGAGGCCACGGATGAG CTGGACCTCAAGCTGCGCCAAGCTGAGGTGATCAAGG GATCCTGGCAGCCCGTGGGCGATCTCCTCATTGACTCT CTCCAAGATCACCTCGAGAAAGTCAAGGCACTTCGAG GAGAAATTGCGCCTCTGAAAGAGAACGTGAGCCACGT CAATGACCTTGCTCGCCAGCTTACCACTTTGGGCATTC AGCTCTCACCGTATAACCTCAGCACTCTGGAAGACCTG AACACCAGATGGAAGCTTCTGCAGGTGGCCGTCGAGG ACCGAGTCAGGCAGCTGCATGAAGCCCACAGGGACTT TGGTCCAGCATCTCAGCACTTTCTTTCCACGTCTGTCCA GGGTCCCTGGGAGAGAGCCATCTCGCCAAACAAAGTG CCCTACTATATCAACCACGAGACTCAAACAACTTGCTG GGACCATCCCAAAATGACAGAGCTCTACCAGTCTTTAG CTGACCTGAATAATGTCAGATTCTCAGCTTATAGGACT GCCATGAAACTCCGAAGACTGCAGAAGGCCCTTTGCTT GGATCTCTTGAGCCTGTCAGCTGCATGTGATGCCTTGG ACCAGCACAACCTCAAGCAAAATGACCAGCCCATGGA TATCCTGCAGATTATTAATTGTTTGACCACTATTTATGA CCGCCTGGAGCAAGAGCACAACAATTTGGTCAACGTC CCTCTCTGCGTGGATATGTGTCTGAACTGGCTGCTGAA TGTTTATGATACGGGACGAACAGGGAGGATCCGTGTC CTGTCTTTTAAAACTGGCATCATTTCCCTGTGTAAAGCA CATTTGGAAGACAAGTACAGATACCTTTTCAAGCAAGT GGCAAGTTCAACAGGATTTTGTGACCAGCGCAGGCTG GGCCTCCTTCTGCATGATTCTATCCAAATTCCAAGACA GTTGGGTGAAGTTGCATCCTTTGGGGGCAGTAACATT GAGCCAAGTGTCCGGAGCTGCTTCCAATTTGCTAATAA TAAGCCAGAGATCGAAGCGGCCCTCTTCCTAGACTGG ATGAGACTGGAACCCCAGTCCATGGTGTGGCTGCCCG TCCTGCACAGAGTGGCTGCTGCAGAAACTGCCAAGCA TCAGGCCAAATGTAACATCTGCAAAGAGTGTCCAATCA TTGGATTCAGGTACAGGAGTCTAAAGCACTTTAATTAT GACATCTGCCAAAGCTGCTTTTTTTCTGGTCGAGTTGC AAAAGGCCATAAAATGCACTATCCCATGGTGGAATATT GCACTCCGACTACATCAGGAGAAGATGTTCGAGACTTT GCCAAGGTACTAAAAAACAAATTTCGAACCAAAAGGT ATTTTGCGAAGCATCCCCGAATGGGCTACCTGCCAGTG CAGACTGTCTTAGAGGGGGACAACATGGAAACTCCCG TTACTCTGATCAACTTCTGGCCAGTAGATTCTGCGCCTG CCTCGTCCCCTCAGCTTTCACACGATGATACTCATTCAC GCATTGAACATTATGCTAGCAGGCTAGCAGAAATGGA AAACAGCAATGGATCTTATCTAAATGATAGCATCTCTC CTAATGAGAGCATAGATGATGAACATTTGTTAATCCAG CATTACTGCCAAAGTTTGAACCAGGACTCCCCCCTGAG CCAGCCTCGTAGTCCTGCCCAGATCTTGATTTCCTTAGA GAGTGAGGAAAGAGGGGAGCTAGAGAGAATCCTAGC AGATCTTGAGGAAGAAAACAGGAATCTGCAAGCAGAA TATGACCGTCTAAAGCAGCAGCACGAACATAAAGGCC TGTCCCCACTGCCGTCCCCTCCTGAAATGATGCCCACCT CTCCCCAGAGTCCCCGGGATGCTGAGCTCATTGCTGAG GCCAAGCTACTGCGTCAACACAAAGGCCGCCTGGAAG CCAGGATGCAAATCCTGGAAGACCACAATAAACAGCT GGAGTCACAGTTACACAGGCTAAGGCAGCTGCTGGAG CAACCCCAGGCAGAGGCCAAAGTGAATGGCACAACG GTGTCCTCTCCTTCTACCTCTCTACAGAGGTCCGACAGC AGTCAGCCTATGCTGCTCCGAGTGGTTGGCAGTCAAAC TTCGGACTCCATGGGTGAGGAAGATCTTCTCAGTCCTC CCCAGGACACAAGCACAGGGTTAGAGGAGGTGATGG AGCAACTCAACAACTCCTTCCCTAGTTCAAGAGGAAGA AATACCCCTGGAAAGCCAATGAGAGAGGACACAATG G17195. 69145970 58109543 InFrame 8313 ATGCCACTCCTGGGTCAGACGGTGAGGTCGGCGTCTG TCGA-06- CGAGGACGCGGCGGTGGAGTAGAAGGGCAGCCGGA 0138- GACAGGCCCGGCGCCCCTTCCGAGGCTAGACGGCCCC 01A-02R- AGCTTCGCGGGGATCATGGCATTGTGGACCGAGTGCG 1849- GGGCCACTGGCGAATCGCCGGCTCCTGTTCAACCTGCT 01.2 GGTGTCCATCTGCATTGTGTTCCTCAACAAATGGATTT ATGTGTACCTTCCCCAACATGAGCCTGACCCTGGTGCA CTTCGTGGTCACCTGGCTGGGCTTGTATATCTGCCAGA AGCTGGACATCTTTGCCCCCAAAAGTCTGCCGCCCTCC AGGCTCCTCCTCCTGGCCCTCAGCTTCTGTGGCTTTGTG GTCTTCACTAACCTTTCTCTGCAGAACAACACCATAGG CACCTATCAGCTGGCCAAGGCCATGACCACGCCGGTG ATCATAGCCATCCAGACCTTCTGCTACCAGAAAACCTT CTCCACCAGAATCCAGCTCACGCTGATTCCTATAACTTT AGGTGTAATCCTAAATTCTTATTACGATGTGAAGTTTA ATTTCCTTGGAATGGTGTTTGCTGCTCTTGGTGTTTTAG TTACATCCCTTTATCAAGTGTGGGTAGGAGCCAAACAG CATGAATTACAAGTGAACTCAATGCAGCTGCTGTACTA CCAGGCTCCGATGTCATCTGCCATGTTGCTGGTTGCTG TGCCCTTCTTTGAGCCAGTGTTTGGAGAAGGAGGAAT ATTTGGTCCCTGGTCAGTTTCTGCTTTG|TTCCTCTGTG ACGAGGGTGCAGGTATCTCTGGGGACTACATCGATCG CGTGGACGAGCCCTTGTCCTGCTCTTATGTGCTGACCA TTCGCACTCCTCGGCTCTGCCCCCACCCTCTCCTCCGGC CCCCACCCAGTGCTGCACCGCAGGCCATCCTCTGTCAC CCTTCCCTACAGCCTGAGGAGTACATGGCCTACGTTCA GAGGCAAGCCGACTCAAAGCAGTATGGAGATAAAATC ATAGAGGAGCTGCAAGATCTAGGCCCCCAAGTGTGGA GTGAGACCAAGTCTGGGGTGGCACCCCAAAAGATGGC AGGTGCGAGCCCGACCAAGGATGACAGTAAGGACTCA GATTTCTGGAAGATGCTTAATGAGCCAGAGGACCAGG CCCCAGGAGGGGAGGAGGTGCCGGCTGAGGAGCAGG ACCCAAGCCCTGAGGCAGCAGATTCAGCTTCTGGTGCT CCCAATGATTTTCAGAACAACGTGCAGGTCAAAGTCAT TCGAAGCCCTGCGGATTTGATTCGATTCATAGAGGAGC TGAAAGGTGGAACAAAAAAGGGGAAGCCAAATATAG GCCAAGAGCAGCCTGTGGATGATGCTGCAGAAGTCCC TCAGAGGGAACCAGAGAAGGAAAGGGGTGATCCAGA ACGGCagagagagatggaagaagaggaggatgaggaatggatg aggatgaagatgaggatgaACGGCAGTTACTGGGAGAATTT GAGAAGGAACTGGAAGGGATCCTGCTTCCGTCAGACC GAGACCGGCTCCGTTCGGAGGTGAAGGCTGGCATGG AGCGGGAACTGGAAAACATCATCCAGGAGACAGAGA AAGAGCTGGACCCAGATGGGCTGAAGAAGGAGTCAG AGCGGGATCGGGCAATGCTGGCTCTCACATCCACTCTC AACAAACTCATCAAAAGACTGGAGGAAAAACAGAGTC CAGAGCTGGTGAAGAAGCACAAGAAAAAGAGGGTTG TCCCCAAAAAGCCTCCCCCATCACCCCAACCTACAGAG GAGGATCCTGAGCACAGAGTCCGGGTCCGGGTCACCA AGCTCCGTCTCGGAGGCCCTAATCAGGATCTGACTGTC CTCGAGATGAAACGGGAAAACCCACAGCTGAAACAAA TCGAGGGGCTGGTGAAGGAGCTGCTGGAGAGGGAGG GACTCACAGCTGCAGGGAAAATTGAGATCAAAATTGT CCGCCCATGGGCTGAAGGGACTGAAGAGGGTGCACG TTGGCTGACTGATGAGGACACGAGAAACCTCAAGGAG ATCTTCTTCAATATCTTGGTGCCGGGAGCTGAAGAGGC CCAGAAGGAACGCCAGCGGCAGAAAGAGCTGGAGAG CAATTACCGCCGGGTGTGGGGCTCTCCAGGTGGGGAG GGCACAGGGGACCTGGACGAATTTGACTTC G17212. 140858113 163956014 InFrame 8314 ATGGTCCCAGAGGCCTGGAGGAGCGGACTGGTAAGC TCGA-06- ACCGGGAGGGTAGTGGGAGTTTTGCTTCTGCTTGGTG 0129- CCTTGAACAAGGCTTCCACGGTCATTCACTATGAGATC 01A-01R- CCGGAGGAAAGAGAGAAGGGTTTCGCTGTGGGCAAC 1849- GTGGTCGCGAACCTTGGTTTGGATCTCGGTAGCCTCTC 01.2 AGCCCGCAGGTTCCGGGTGGTGTCTGGAGCTAGCCGA AGATTCTTTGAGGTGAACCGGGAGACCGGAGAGATGT TTGTGAACGACCGTCTGGATCGAGAGGAGCTGTGTGG GACACTGCCCTCTTGCACTGTAACTCTGGAGTTGGTAG TGGAGAACCCGCTGGAGCTGTTCAGCGTGGAAGTGGT GATCCAGGACATCAACGACAACAATCCTGCTTTCCCTA CCCAGGAAATGAAATTGGAGATTAGCGAGGCCGTGGC TCCGGGGACGCGCTTTCCGCTCGAGAGCGCGCACGAT CCCGATGTGGGAAGCAACTCTTTACAAACCTATGAGCT GAGCCGAAATGAATACTTTGCGCTTCGCGTGCAGACG CGGGAGGACAGCACCAAGTACGCGGAGCTGGTGTTG GAGCGCGCCCTGGACCGAGAACGGGAGCCTAGTCTCC AGTTAGTGCTGACGGCGTTGGACGGAGGGACCCCAGC TCTCTCCGCCAGCCTGCCTATTCACATCAAGGTGCTGG ACGCGAATGACAATGCGCCTGTCTTCAACCAGTCCTTG TACCGGGCGCGCGTCCTGGAGGATGCACCCTCCGGCA CGCGCGTGGTACAAGTCCTTGCAACGGATCTGGATGA AGGCCCCAACGGTGAAATTATTTACTCCTTCGGCAGCC ACAACCGCGCCGGCGTGCGGCAACTATTCGCCTTAGA CCTTGTAACCGGGATGCTGACAATCAAGGGTCGGCTG GACTTCGAGGACACCAAACTCCATGAGATTTACATCCA GGCCAAAGACAAGGGCGCCAATCCCGAAGGAGCACA TTGCAAAGTGTTGGTGGAGGTTGTGGATGTGAATGAC AACGCCCCGGAGATCACAGTCACCTCCGTGTACAGCCC AGTACCCGAGGATGCCCCTCTGGGGACTGTCATCGCTT TGCTCAGTGTGACTGACCTGGATGCTGGCGAGAACGG GCTGGTGACCTGCGAAGTTCCACCGGGTCTCCCTTTCA GCCTTACTTCTTCCCTCAAGAATTACTTCACTTTGAAAA CCAGTGCAGACCTGGATCGGGAGACTGTGCCAGAATA CAACCTCAGCATCACCGCCCGAGACGCCGGAACCCCTT CCCTCTCAGCCCTTACAATAGTGCGTGTTCAAGTGTCC GACATCAATGACAACCCTCCACAATCTTCTCAATCTTCC TACGACGTTTACATTGAAGAAAACAACCTCCCCGGGGC TCCAATACTAAACCTAAGTGTCTGGGACCCCGACGCCC CGCAGAATGCTCGGCTTTCTTTCTTTCTCTTGGAGCAA GGAGCTGAAACCGGGCTAGTGGGTCGCTATTTCACAA TAAATCGTGACAATGGCATAGTGTCATCCTTAGTGCCC CTAGACTATGAGGATCGGCGGGAATTTGAATTAACAG CTCATATCAGCGATGGGGGCACCCCGGTCCTAGCCACC AACATCAGCGTGAACATATTTGTCACTGATCGCAATGA CAATGCCCCCCAGGTCCTATATCCTCGGCCAGGTGGGA GCTCGGTGGAGATGCTGCCTCGAGGTACCTCAGCTGG CCACCTAGTGTCACGGGTGGTAGGCTGGGACGCGGAT GCAGGGCACAATGCCTGGCTCTCCTACAGTCTCTTGGG ATCCCCTAACCAGAGCCTTTTTGCCATAGGGCTGCACA CTGGTCAAATCAGTACTGCCCGTCCAGTCCAAGACACA GATTCACCCAGGCAGACTCTCACGGTCTTGATCAAAGA CAATGGGGAGCCTTCGCTCTCCACCACTGCTACCCTCA CTGTGTCAGTAACCGAGGACTCTCCTGAAGCCCGAGCC GAGTTCCCCTCTGGCTCTGCCCCCCGGGAGCAGAAAA AAAATCTCACCTTTTATCTACTTCTTTCTCTAATCCTGGT TTCTGTGGGGTTTGTGGTCACAGTGTTCGGAGTAATCA TATTCAAAGTTTACAAGTGGAAGCAGTCTAGAGACCTA TACCGAGCCCCGGTGAGCTCACTGTACCGAACACCAG GGCCCTCCTTGCACGCGGACGCCGTGCGGGGAGGCCT GATGTCGCCGCACCTTTACCATCAGGTGTATCTCACCA CGGACTCCCGCCGCAGCGACCCGCTGCTGAAGAAACC TGGTGCAGCCAGTCCACTGGCCAGCCGCCAGAACACG CTGCGGAGCTGTGATCCGGTGTTCTATAGGCAGGTGT TGGGTGCAGAGAGCGCCCCTCCCGGACAG|GAGGAG CAAAATAGAGGCAAGCCCAATTGGGAGCATCTAAATG AAGATTTACATGTACTAATCACTGTGGAAGATGCTCAG AACAGAGCAGAAATCAAATTGAAGAGAGCAGTTGAAG AAGTGAAGAAATTATTGGTACCTGCAGCAGAAGGAGA AGACAGCCTGAAGAAGATGCAGCTGATGGAGCTTGCG ATTCTGAATGGCACCTACAGAGATGCCAACATTAAATC ACCAGCCCTTGCCTTTTCTCTTGCAGCAACAGCCCAGG CTGCTCCAAGGATCATTACTGGGCCTGCGCCGGTTCTC CCACCAGCTGCCCTGCGTACTCCTACGCCAGCTGGCCC TACCATAATGCCTTTGATCAGACAAATACAGACCGCTG TCATGCCAAACGGAACTCCTCACCCAACTGCTGCAATA GTTCCTCCAGGGCCCGAAGCTGGTTTAATCTATACACC CTATGAGTACCCCTACACATTGGCACCAGCTACATCAA TCCTTGAGTATCCTATTGAACCTAGTGGTGTATTAGGT GCGGTGGCTACTAAAGTTCGAAGGCACGATATGCGTG TCCATCCTTACCAAAGGATTGTGACCGCAGACCGAGCC GCCACCGGCAAC G17213. 2062889 90075838 InFrame 8315 ATGGCGGACATCGAGCAGTACTACATGAAGCCGCCCG TCGA-06- |AGATCGTTAAGGAGGCTGAGGTGCCGCAGGCTGCGC 0157- TGGGCGTCCCAGCCCAGGGGACAGGGGACAATGGCC 01A-01R- ACACGCCTGTGGAGGAGGAGGTCGGGGGCATCCCAG 1849- TACCAGCACCGGGGCTCCTGCAGGTCACGGAGAGGAG 01.2 GCAGCCTCTGAGCAGCGTCTCCTCTCTGGAGGTCCACT TCGACCTCCTGGACCTCACTGAGCTCACCGACATGTCG GACCAGGAGCTGGCCGAGGTCTTTGCTGACTCGGACG ACGAGAACCTCAACACCGAGTCCCCAGCAGGTCTGCA CCCGCTGCCCCGGGCCGGCTACCTGCGCTCCCCTTCCT GGACGAGGACAAGGGCTGAGCAGAGCCACGAGAAGC AGCCCCTAGGCGACCCCGAGCGGCAGGCCACAGTCCT GGACACGTTTCTCACTGTGGAGAGGCCCCAGGAGGAC G17200. 27094490 24624366 InFrame 8316 ATGGCCGCGCAGGTCGCCCCCGCCGCCGCCAGCAGCC TCGA-06- TGGGCAACCCGCCGCCGCCGCCGCCCTCGGAGCTGAA 0125- GAAAGCCGAgcagcagcagcgggaggaggcggggggcgaggcg 01A-01R- gcggcggcggcagcggcCGAGCGCGGGGAAATGAAGGCA 1849- GCCGCCGGGCAGGAAAGCGAGGGCCCCGCCGTGGGG 01.2 CCGCCGCAGCCGCTGGGAAAGGAGCTGCAGGACGGG GCCGAGAGCAATGGGggtggcggcggcggcggacccagc ggcggcggGCCCGGCGCGGAGCCGGACCTGAAGAACTC GAACGGGAACGCGGGCCCTAGGCCCGCCCTGAACAAT AACCTCACGGAGCCGCCcggcggcggcggtggcggcagcagc gatggggtgggggcgCCTCCTCACTCAGCCGCGGCCGCCTT GCCGCCCCCAGCCTACGGCTTCGGGCAACCCTACGGCC GGAGCCCGTCTGCCGTCGCCGCCGCCGCGGCCGCCGT CTTCCACCAACAACATGGCGGACAACAAAGCCCTGGC CTGGCAGCGCTGCAGAGCGGCGGCGGCGGGGGCCTG GAGCCCTACGCGGGGCCCCAGCAGAACTCTCACGACC ACGGCTTCCCCAACCACCAGTACAACTCCTACTACCCC AACCGCAGCGCCTACCCCCCGCCCGCCCCGGCCTACGC GCTGAGCTCCCCGAGAGGTGGCACTCCGGGCTCCGGC GCGGCGGCGGCTGCCGGCTCCAAGCCGCCTCCCTCCTC CAGCGCCTCCGCCTCCTCGTCGTCTTCGTCCTTCGCTCA GCAGCGCTTCGGGGCCATGGGGGGAGGCGGCCCCTC CGCGGCCGGCGGGGGAACTCCCCAGCCCACCGCCACC CCCACCCTCAACCAACTGCTCACGTCGCCCAGCTCGGC CCGGGGCTACCAGGGCTACCCCGGGGGCGACTACAGT GGCGGGCCCCAGGACGGGGGCGCCGGCAAGGGCCCG GCGGACATGGCCTCGCAGTGTTGGGGggctgcggcggcgg cagctgcggcggcggcCGCCTCGGGAGGGGCCCAACAAAG GAGCCACCACGCGCCCATGAGCCCCGGGAGCAGCGGC GGCGGGGGGCAGCCGCTCGCCCGGACCCCTCAGCCAT CCAGTCCAATGGATCAGATGGGCAAGATGAGACCTCA GCCATATGGCGGGACTAACCCATACTCGCAGCAACAG GGACCTCCGTCAGGACCGCAGCAAGGACATGGGTACC CAGGGCAGCCATACGGGTCCCAGACCCCGCAGCGGTA CCCGATGACCATGCAGGGCCGGGCGCAGAGTGCCATG GGCGGCCTCTCTTATACACAGCAGATTCCTCCTTATGG ACAACAAGGCCCCAGCGGGTATGGTCAACAGGGCCAG ACTCCATATTACAACCAGCAAAGTCCTCACCCTCAGCA GCAGCAGCCACCCTACTCCCAGCAACCACCGTCCCAGA CCCCTCATGCCCAACCTTCGTATCAGCAGCAGCCACAG TCTCAACCACCACAGCTCCAGTCCTCTCAGCCTCCATAC TCCCAGCAGCCATCCCAGCCTCCACATCAGCAGTCCCC GGCTCCATACCCCTCCCAGCAGTCGACGACACAGCAGC ACCCCCAGAGCCAGCCCCCCTACTCACAGCCACAGGCT CAGTCTCCTTACCAGCAGCAGCAACCTCAGCAGCCAGC ACCCTCGACGCTCTCCCAGCAGGCTGCGTATCCTCAGC CCCAGTCTCAGCAGTCCCAGCAAACTGCCTATTCCCAG CAGCGCTTCCCTCCACCGCAGGAGCTATCTCAAGATTC ATTTGGGTCTCAGGCATCCTCAGCCCCCTCAATGACCT CCAGTAAGGGAGGGCAAGAAGATATGAACCTGAGCCT TCAGTCAAGACCCTCCAGCTTGCCTGATCTATCTGGTTC AATAGATGACCTCCCCATGGGGACAGAAGGAGCTCTG AGTCCTGGAGTGAGCACATCAGGGATTTCCAGCAGCC AAGGAGAGCAGAGTAATCCAGCTCAGTCTCCTTTCTCT CCTCATACCTCCCCTCACCTGCCTGGCATCCGAGGCCCT TCCCCGTCCCCTGTTGGCTCTCCCGCCAGTGTTGCTCAG TCTCGCTCAGGACCACTCTCGCCTGCTGCAGTGCCAGG CAACCAGATGCCACCTCGGCCACCCAGTGGCCAGTCG GACAGCATCATGCATCCTTCCATGAACCAATCAAGCAT TGCCCAAGATCGAGGTTATATGCAGAGGAACCCCCAG ATGCCCCAGTACAGTTCCCCCCAGCCCGGCTCAGCCTT ATCTCCGCGTCAGCCTTCCGGAGGACAGATACACACA GGCATGGGCTCCTACCAGCAGAACTCCATGGGGAGCT ATGGTCCCCAGGGGGGTCAGTATGGCCCACAAGGTGG CTACCCCAGGCAGCCAAACTATAATGCCTTGCCCAATG CCAACTACCCCAGTGCAGGCATGGCTGGAGGCATAAA CCCCATGGGTGCCGGAGGTCAAATGCATGGACAGCCT GGCATCCCACCTTATGGCACACTCCCTCCAGGGAGGAT GAGTCACGCCTCCATGGGCAACCGGCCTTATGGCCCTA ACATGGCCAATATGCCACCTCAGGTTGGGTCAGGGAT GTGTCCCCCACCAGGGGGCATGAACCGGAAAACCCAA GAAACTGCTGTCGCCATGCATGTTGCTGCCAACTCTAT CCAAAACAGGCCGCCAGGCTACCCCAATATGAATCAA GGGGGCATGATGGGAACTGGACCTCCTTATGGACAAG GGATTAATAGTATGGCTGGCATGATCAACCCTCAGGG ACCCCCATATTCCATGGGTGGAACCATGGCCAACAATT CTGCAGGGATGGCAGCCAGCCCAGAGATGATGGGCCT TGGGGATGTAAAGTTAACTCCAGCCACCAAAATGAAC AACAAGGCAGATGGGACACCCAAGACAGAATCCAAAT CCAAGAAATCCAGTTCTTCTACTACAACCAATGAGAAG ATCACCAAGTTGTATGAGCTGGGTGGTGAGCCTGAGA GGAAGATGTGGGTGGACCGTTATCTGGCCTTCACTGA GGAGAAGGCCATGGGCATGACAAATCTGCCTGCTGTG GGTAGGAAACCTCTGGACCTCTATCGCCTCTATGTGTC TGTGAAGGAGATTGGTGGATTGACTCAG|ATGCAGGC CCTGACTTCCTGTGAGTGCACCATCTGTCCTGACTGCTT CCGCCAGCACTTCACCATCGCCTTGAAGGAGAAGCAC ATCACAGACATGGTGTGCCCTGCCTGTGGCCGCCCCGA CCTCACCGATGACACACAGTTGCTCAGCTACTTCTCTAC CCTTGACATCCAGCTTCGCGAGAGCCTAGAGCCAGAT GCCTATGCGTTGTTCCATAAGAAGCTGACCGAGGGTG TGCTGATGCGGGACCCCAAGTTCTTGTGGTGTGCCCAG TGCTCCTTTGGCTTCATATATGAGCGTGAGCAGCTGGA GGCAACTTGTCCCCAGTGTCACCAGACCTTCTGTGTGC GCTGCAAGCGCCAGTGGGAGGAGCAGCACCGAGGTC GGAGCTGTGAGGACTTCCAGAACTGGAAACGCATGAA CGACCCAGAATACCAGGCCCAGGGCCTAGCAATGTAT CTTCAGGAAAACGGCATTGACTGCCCCAAATGCAAGTT CTCGTACGCCCTGGCCCGAGGAGGCTGCATGCACTTTC ACTGTACCCAGTGCCGCCACCAGTTCTGCAGCGGCTGC TACAATGCCTTTTACGCCAAGAATAAATGTCCAGAGCC TAACTGCAGGGTGAAAAAGTCCCTGCACGGCCACCAC CCTCGAGACTGCCTCTTCTACCTGCGGGACTGGACTGC TCTCCGGCTTCAGAAGCTGCTACAGGACAATAACGTCA TGTTTAATACAGAGCCTCCAGCTGGGGCCCGGGCAGT CCCTGGAGGCGGCTGCCGAGTGATAGAGCAGAAGGA GGTTCCCAATGGGCTCAGGGACGAAGCTTGTGGCAAG GAAACTCCAGCTGGCTATGCCGGCCTGTGCCAGGCAC ACTACAAAGAGTATCTTGTGAGCCTCATCAATGCCCAC TCGCTGGACCCAGCCACCTTGTATGAGGTGGAAGAGC TGGAGACGGCCACTGAGCGCTACCTGCACGTACGCCC CCAGCCTTTGGCTGGAGAGGATCCCCCTGCTTACCAGG CCCGCTTGTTACAGAAGCTGACAGAAGAGGTACCCTT GGGACAGAGTATCCCCCGCAGGCGGAAG G17804. 55268105 56079562 InFrame 8317 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-06- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 5408- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01A-01R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1849- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.4 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAG|GATGCT TTCATTGGATTTGGAGGAAATGTGATCAGGCAACAAG TCAAGGATAACGCCAAATGGTATATCACTGATTTTGTA GAGCTGCTGGGAGAACTGGAAGAA G17656. 27024031 49202124 InFrame 8318 ATGGCCGCGCAGGTCGCCCCCGCCGCCGCCAGCAGCC TCGA-28- TGGGCAACCCGCCGCCGCCGCCGCCCTCGGAGCTGAA 2514- GAAAGCCGAgcagcagcagcgggaggaggcggggggcgaggcg 01A-02R- gcggcggcggcagcggcCGAGCGCGGGGAAATGAAGGCA 1850- GCCGCCGGGCAGGAAAGCGAGGGCCCCGCCGTGGGG 01.2 CCGCCGCAGCCGCTGGGAAAGGAGCTGCAGGACGGG GCCGAGAGCAATGGGggtggcggcggcggcggagccggcagc ggcggcggGCCCGGCGCGGAGCCGGACCTGAAGAACTC GAACGGGAACGCGGGCCCTAGGCCCGCCCTGAACAAT AACCTCACGGAGCCGCCcggcggcggcggtggcggcagcagc gatggggtgggggcgCCTCCTCACTCAGCCGCGGCCGCCTT GCCGCCCCCAGCCTACGGCTTCGGGCAACCCTACGGCC GGAGCCCGTCTGCCGTCGCCGCCGCCGCGGCCGCCGT CTTCCACCAACAACATGGCGGACAACAAAGCCCTGGC CTGGCAGCGCTGCAGAGCGGCGGCGGCGGGGGCCTG GAGCCCTACGCGGGGCCCCAGCAGAACTCTCACGACC ACGGCTTCCCCAACCACCAGTACAACTCCTACTACCCC AACCGCAGCGCCTACCCCCCGCCCGCCCCGGCCTACGC GCTGAGCTCCCCGAGAGGTGGCACTCCGGGCTCCGGC GCGGCGGCGGCTGCCGGCTCCAAGCCGCCTCCCTCCTC CAGCGCCTCCGCCTCCTCGTCGTCTTCGTCCTTCGCTCA GCAGCGCTTCGGGGCCATGGGGGGAGGCGGCCCCTC CGCGGCCGGCGGGGGAACTCCCCAGCCCACCGCCACC CCCACCCTCAACCAACTGCTCACGTCGCCCAGCTCGGC CCGGGGCTACCAGGGCTACCCCGGGGGCGACTACAGT GGCGGGCCCCAGGACGGGGGCGCCGGCAAGGGCCCG GCGGACATGGCCTCGCAGTGTTGGGGggctgcggcggcgg cagctgcggcggcggcCGCCTCGGGAGGGGCCCAACAAAG GAGCCACCACGCGCCCATGAGCCCCGGGAGCAGCGGC GGCGGGGGGCAGCCGCTCGCCCGGACCCCTCAGTGTC CATCTGGGAAGCGGGATTTGGGTTGATGAGGAGAAAT GGCACCAGCTACAAGTAACCCAAGGAGATTCCAAGTA CACGAAGAACTTGGCAGTTATGATTTGGGGAACAGAT GTTCTGAAAAACAGAAGCGTCACAGGCGTCGCCACAA AAAAAAAGAAAGATGCAGTCCCTAAACCACCCCTCTCG CCTCACAAACTAAGCATCGTCAGAGAGTGTTTGTATGA CAGAATAGCACAAGAAACTGTGGATGAAACTGAAATT GCACAGAGACTCTCCAAAGTCAACAAGTACATCTGTGA AAAAATCATGGATATCAATAAATCCTGTAAAAATGAAG AACGAAGGGAAGCAAAATACAATTTGCAA G17654. 146017814 156294880 InFrame 8319 ATGCTTCTCTCGTTACCTGCCTTACATCTTCAGACCTCC TCGA-41- GAACACCATCCTTTCTTCCAGCTGCCACACAGAAGGCT 4097- CGGACCATGGTGCAGTCCCACTGGCTCCCCTGCCCCCC 01A-01R- TCTCCTGTGAGACTGGCTGCGGGGAGGGATCATGGAT 1850- ACTTGTCTGCCGGCTTCTGGTTCCCACGCAAGTAAGCC 01.2 TGCTGTCAATGGAGGAGGACATTGATACCCGCAAAAT CAACAACAGTTTCCTGCGCGACCACAGCTATGCGACCG AAGCTGACATTATCTCTACGGTAGAATTCAACCACACG GGAGAATTACTAGCGACAGGGGACAAGGGGGGTCGG GTTGTAATATTTCAACGAGAGCAGGAGAGTAAAAATC AGGTTCATCGTAGGGGTGAATACAATGTTTACAGCAC ATTCCAGAGCCATGAACCCGAGTTCGATTACCTGAAGA GTTTAGAAATAGAAGAAAAAATCAATAAAATAAGATG GCTCCCCCAGCAGAATGCAGCTTACTTTCTTCTGTCTAC TAATGATAAAACTGTGAAGCTGTGGAAAGTCAGCGAG CGTGATAAGAGGCCAGAAGGCTACAATCTGAAAGATG AGGAGGGCCGGCTCCGGGATCCTGCCACCATCACAAC CCTGCGGGTGCCTGTCCTGAGACCCATGGACCTGATG GTGGAGGCCACCCCACGAAGAGTATTTGCCAACGCAC ACACATATCACATCAACTCCATATCTGTCAACAGCGAC TATGAAACCTACATGTCCGCTGATGACCTGAGGATTAA CCTATGGAACTTTGAAATAACCAATCAAAGTTTTAATA TTGTGGACATTAAGCCAGCCAACATGGAGGAGCTCAC GGAGGTGATCACAGCAGCCGAGTTCCACCCCCATCATT GCAACACCTTCGTGTACAGCAGCAGCAAAGGGACAAT CCGGCTGTGTGACATGCGGGCATCTGCCCTGTGTGAC AGGCACACCAAAT|CAGGGGAAATGCTGTCTGTAGCT GAGCACTTCCTGGAGCAGCAGATGCACCCAACAGTGG TGATCAGTGCTTACCGCAAGGCATTGGATGATATGATC AGCACCCTAAAGAAAATAAGTATCCCAGTCGACATCAG TGACAGTGATATGATGCTGAACATCATCAACAGCTCTA TTACTACCAAAGCCATCAGTCGGTGGTCATCTTTGGCT TGCAACATTGCCCTGGATGCTGTCAAGATGGTACAGTT TGAGGAGAATGGTCGGAAAGAGATTGACATAAAAAA ATATGCAAGAGTGGAAAAGATACCTGGAGGCATCATT GAAGACTCCTGTGTCTTGCGTGGAGTCATGATTAACAA GGATGTGACCCATCCACGTATGCGGCGCTATATCAAG AACCCTCGCATTGTGCTGCTGGATTCTTCTCTGGAATAC AAGAAAGGAGAAAGCCAGACTGACATTGAGATTACAC GAGAGGAGGACTTCACCCGAATTCTCCAGATGGAGGA AGAGTACATCCAGCAGCTCTGTGAGGACATTATCCAAC TGAAGCCCGATGTGGTCATCACTGAAAAGGGCATCTC AGATTTAGCTCAGCACTACCTTATGCGGGCCAATATCA CAGCCATCCGCAGAGTCCGGAAGACAGACAATAATCG CATTGCTAGAGCCTGTGGGGCCCGGATAGTCAGCCGA CCAGAGGAACTGAGAGAAGATGATGTTGGAACAGGA GCAGGCCTGTTGGAAATCAAGAAAATTGGAGATGAAT ACTTTACTTTCATCACTGACTGCAAAGACCCCAAGGCC TGCACCATTCTCCTCCGGGGGGCTAGCAAAGAGATTCT CTCGGAAGTAGAACGCAACCTCCAGGATGCCATGCAA GTGTGTCGCAATGTTCTCCTGGACCCTCAGCTGGTGCC AGGGGGTGGGGCCTCCGAGATGGCTGTGGCCCATGCC TTGACAGAAAAATCCAAGGCCATGACTGGTGTGGAAC AATGGCCATACAGGGCTGTTGCCCAGGCCCTAGAGGT CATTCCTCGTACCCTGATCCAGAACTGTGGGGCCAGCA CCATCCGTCTACTTACCTCCCTTCGGGCCAAGCACACCC AGGAGAACTGTGAGACCTGGGGTGTAAATGGTGAGA CGGGTACTTTGGTGGACATGAAGGAACTGGGCATATG GGAGCCATTGGCTGTGAAGCTGCAGACTTATAAGACA GCAGTGGAGACGGCAGTTCTGCTACTGCGAATTGATG ACATCGTTTCAGGCCACAAAAAGAAAGGCGATGACCA GAGCCGGCAAGGCGGGGCTCCTGATGCTGGCCAGGA G G17206. 27094490 24624366 InFrame 8320 ATGGCCGCGCAGGTCGCCCCCGCCGCCGCCAGCAGCC TCGA-06- TGGGCAACCCGCCGCCGCCGCCGCCCTCGGAGCTGAA 0125- GAAAGCCGAgcagcagcagcgggaggaggcggggggcgaggcg 02A-11R- gcggcggcggcagcggcCGAGCGCGGGGAAATGAAGGCA 2005- GCCGCCGGGCAGGAAAGCGAGGGCCCCGCCGTGGGG 01.2 CCGCCGCAGCCGCTGGGAAAGGAGCTGCAGGACGGG GCCGAGAGCAATGGGggtggcggcggcggcggacccagc ggcggcggGCCCGGCGCGGAGCCGGACCTGAAGAACTC GAACGGGAACGCGGGCCCTAGGCCCGCCCTGAACAAT AACCTCACGGAGCCGCCcggcggcggcggtggcggcagcagc gatggggtgggggcgCCTCCTCACTCAGCCGCGGCCGCCTT GCCGCCCCCAGCCTACGGCTTCGGGCAACCCTACGGCC GGAGCCCGTCTGCCGTCGCCGCCGCCGCGGCCGCCGT CTTCCACCAACAACATGGCGGACAACAAAGCCCTGGC CTGGCAGCGCTGCAGAGCGGCGGCGGCGGGGGCCTG GAGCCCTACGCGGGGCCCCAGCAGAACTCTCACGACC ACGGCTTCCCCAACCACCAGTACAACTCCTACTACCCC AACCGCAGCGCCTACCCCCCGCCCGCCCCGGCCTACGC GCTGAGCTCCCCGAGAGGTGGCACTCCGGGCTCCGGC GCGGCGGCGGCTGCCGGCTCCAAGCCGCCTCCCTCCTC CAGCGCCTCCGCCTCCTCGTCGTCTTCGTCCTTCGCTCA GCAGCGCTTCGGGGCCATGGGGGGAGGCGGCCCCTC CGCGGCCGGCGGGGGAACTCCCCAGCCCACCGCCACC CCCACCCTCAACCAACTGCTCACGTCGCCCAGCTCGGC CCGGGGCTACCAGGGCTACCCCGGGGGCGACTACAGT GGCGGGCCCCAGGACGGGGGCGCCGGCAAGGGCCCG GCGGACATGGCCTCGCAGTGTTGGGGggctgcggcggcgg cagctgcggcggcggcCGCCTCGGGAGGGGCCCAACAAAG GAGCCACCACGCGCCCATGAGCCCCGGGAGCAGCGGC GGCGGGGGGCAGCCGCTCGCCCGGACCCCTCAGCCAT CCAGTCCAATGGATCAGATGGGCAAGATGAGACCTCA GCCATATGGCGGGACTAACCCATACTCGCAGCAACAG GGACCTCCGTCAGGACCGCAGCAAGGACATGGGTACC CAGGGCAGCCATACGGGTCCCAGACCCCGCAGCGGTA CCCGATGACCATGCAGGGCCGGGCGCAGAGTGCCATG GGCGGCCTCTCTTATACACAGCAGATTCCTCCTTATGG ACAACAAGGCCCCAGCGGGTATGGTCAACAGGGCCAG ACTCCATATTACAACCAGCAAAGTCCTCACCCTCAGCA GCAGCAGCCACCCTACTCCCAGCAACCACCGTCCCAGA CCCCTCATGCCCAACCTTCGTATCAGCAGCAGCCACAG TCTCAACCACCACAGCTCCAGTCCTCTCAGCCTCCATAC TCCCAGCAGCCATCCCAGCCTCCACATCAGCAGTCCCC GGCTCCATACCCCTCCCAGCAGTCGACGACACAGCAGC ACCCCCAGAGCCAGCCCCCCTACTCACAGCCACAGGCT CAGTCTCCTTACCAGCAGCAGCAACCTCAGCAGCCAGC ACCCTCGACGCTCTCCCAGCAGGCTGCGTATCCTCAGC CCCAGTCTCAGCAGTCCCAGCAAACTGCCTATTCCCAG CAGCGCTTCCCTCCACCGCAGGAGCTATCTCAAGATTC ATTTGGGTCTCAGGCATCCTCAGCCCCCTCAATGACCT CCAGTAAGGGAGGGCAAGAAGATATGAACCTGAGCCT TCAGTCAAGACCCTCCAGCTTGCCTGATCTATCTGGTTC AATAGATGACCTCCCCATGGGGACAGAAGGAGCTCTG AGTCCTGGAGTGAGCACATCAGGGATTTCCAGCAGCC AAGGAGAGCAGAGTAATCCAGCTCAGTCTCCTTTCTCT CCTCATACCTCCCCTCACCTGCCTGGCATCCGAGGCCCT TCCCCGTCCCCTGTTGGCTCTCCCGCCAGTGTTGCTCAG TCTCGCTCAGGACCACTCTCGCCTGCTGCAGTGCCAGG CAACCAGATGCCACCTCGGCCACCCAGTGGCCAGTCG GACAGCATCATGCATCCTTCCATGAACCAATCAAGCAT TGCCCAAGATCGAGGTTATATGCAGAGGAACCCCCAG ATGCCCCAGTACAGTTCCCCCCAGCCCGGCTCAGCCTT ATCTCCGCGTCAGCCTTCCGGAGGACAGATACACACA GGCATGGGCTCCTACCAGCAGAACTCCATGGGGAGCT ATGGTCCCCAGGGGGGTCAGTATGGCCCACAAGGTGG CTACCCCAGGCAGCCAAACTATAATGCCTTGCCCAATG CCAACTACCCCAGTGCAGGCATGGCTGGAGGCATAAA CCCCATGGGTGCCGGAGGTCAAATGCATGGACAGCCT GGCATCCCACCTTATGGCACACTCCCTCCAGGGAGGAT GAGTCACGCCTCCATGGGCAACCGGCCTTATGGCCCTA ACATGGCCAATATGCCACCTCAGGTTGGGTCAGGGAT GTGTCCCCCACCAGGGGGCATGAACCGGAAAACCCAA GAAACTGCTGTCGCCATGCATGTTGCTGCCAACTCTAT CCAAAACAGGCCGCCAGGCTACCCCAATATGAATCAA GGGGGCATGATGGGAACTGGACCTCCTTATGGACAAG GGATTAATAGTATGGCTGGCATGATCAACCCTCAGGG ACCCCCATATTCCATGGGTGGAACCATGGCCAACAATT CTGCAGGGATGGCAGCCAGCCCAGAGATGATGGGCCT TGGGGATGTAAAGTTAACTCCAGCCACCAAAATGAAC AACAAGGCAGATGGGACACCCAAGACAGAATCCAAAT CCAAGAAATCCAGTTCTTCTACTACAACCAATGAGAAG ATCACCAAGTTGTATGAGCTGGGTGGTGAGCCTGAGA GGAAGATGTGGGTGGACCGTTATCTGGCCTTCACTGA GGAGAAGGCCATGGGCATGACAAATCTGCCTGCTGTG GGTAGGAAACCTCTGGACCTCTATCGCCTCTATGTGTC TGTGAAGGAGATTGGTGGATTGACTCAG|ATGCAGGC CCTGACTTCCTGTGAGTGCACCATCTGTCCTGACTGCTT CCGCCAGCACTTCACCATCGCCTTGAAGGAGAAGCAC ATCACAGACATGGTGTGCCCTGCCTGTGGCCGCCCCGA CCTCACCGATGACACACAGTTGCTCAGCTACTTCTCTAC CCTTGACATCCAGCTTCGCGAGAGCCTAGAGCCAGAT GCCTATGCGTTGTTCCATAAGAAGCTGACCGAGGGTG TGCTGATGCGGGACCCCAAGTTCTTGTGGTGTGCCCAG TGCTCCTTTGGCTTCATATATGAGCGTGAGCAGCTGGA GGCAACTTGTCCCCAGTGTCACCAGACCTTCTGTGTGC GCTGCAAGCGCCAGTGGGAGGAGCAGCACCGAGGTC GGAGCTGTGAGGACTTCCAGAACTGGAAACGCATGAA CGACCCAGAATACCAGGCCCAGGGCCTAGCAATGTAT CTTCAGGAAAACGGCATTGACTGCCCCAAATGCAAGTT CTCGTACGCCCTGGCCCGAGGAGGCTGCATGCACTTTC ACTGTACCCAGTGCCGCCACCAGTTCTGCAGCGGCTGC TACAATGCCTTTTACGCCAAGAATAAATGTCCAGAGCC TAACTGCAGGGTGAAAAAGTCCCTGCACGGCCACCAC CCTCGAGACTGCCTCTTCTACCTGCGGGACTGGACTGC TCTCCGGCTTCAGAAGCTGCTACAGGACAATAACGTCA TGTTTAATACAGAGCCTCCAGCTGGGGCCCGGGCAGT CCCTGGAGGCGGCTGCCGAGTGATAGAGCAGAAGGA GGTTCCCAATGGGCTCAGGGACGAAGCTTGTGGCAAG GAAACTCCAGCTGGCTATGCCGGCCTGTGCCAGGCAC ACTACAAAGAGTATCTTGTGAGCCTCATCAATGCCCAC TCGCTGGACCCAGCCACCTTGTATGAGGTGGAAGAGC TGGAGACGGCCACTGAGCGCTACCTGCACGTACGCCC CCAGCCTTTGGCTGGAGAGGATCCCCCTGCTTACCAGG CCCGCTTGTTACAGAAGCTGACAGAAGAGGTACCCTT GGGACAGAGTATCCCCCGCAGGCGGAAG G17792. 36204176 33911962 InFrame 8321 ATGGCTGAGCTGGATCCGTTCGGCGCCCCTGCCGGCG TCGA-28- CCCCTGGCGGTCCCGCGCTGGGGAACGGAGTGGCCG 5204- GCGCCGGCGAAGAAGACCCGGCTGCGGCCTTCTTGGC 01A-01R- GCAGCAAGAGAGCGAGATTGCGGGCATCGAGAACGA 1850- CGAGGCCTTCGCCATCCTGGAcggcggcgcccccgggcccca 01.4 gccgcacggcgagccgccggggggTCCGGATGCTGTTGATGG AGTAATGAATGGTGAATACTACCAGGAAAGTAATGGT CCAACAGACAGTTATGCAGCTATTTCACAAGTGGATCG ATTGCAGTCAGAGCCTGAAAGTATCCGTAAATGGAGA GAAGAACAAATGGAACGCTTGGAAGCCCTTGATGCCA ATTCTCGGAAGCAAGAAGCAGAGTGGAAAGAAAAGG CAATAAAGGAGCTAGAAGAATGGTATGCAAGACAGG ACGAGCAGCTACAGAAAACAAAAGCAAACAACAG|GA CTATCCTATTAAGTGTAATCTCACTGCTTAATGAGCCCA ACACCTTCTCCCCAGCCAATGTCGATGCTTCAGTTATGT TCAGGAAATGGAGAGACAGTAAAGGAAAAGACAAAG AATATGCTGAAATTATTAGGAAACAAGTTTCAGCCACT AAGGCCGAAGCAGAAAAGGATGGAGTGAAGGTCCCC ACAACCCTGGCGGAATACTGCATCAAAACTAAAGTGC CTTCCAATGACAACAGCTCAGATTTGCTTTACGACGAC TTGTatgatgacgacattgatgatgaagatgaggaggaggaagatgc cgactgttatgatgatgatgatTCTGGGAATGAGGAGTCG G17663. 205719085 205811017 InFrame 8322 ATGTCGCGGCCTGTCAG|GTTTATGGAGAGAAATCCCT TCGA-19- TAACCAATGCAATAATCAGGACCACCACGGCACTCACC 2619- ATATTCAAAGCAGGGGTCAAGTTCAATGTCATCCCCCC 01A-01R- AGTGGCCCAGGCCACAGTCAACTTCCGGATTCACCCTG 1850- GACAGACAGTCCAAGAGGTCCTAGAACTCACGAAGAA 01.2 CATTGTGGCTGATAACAGAGTCCAGTTCCATGTGTTGA GTGCCTTTGACCCCCTCCCCGTCAGCCCTTCTGATGACA AGGCCTTGGGCTACCAGCTGCTCCGCCAGACCGTACA GTCCGTCTTCCCGGAAGTCAATATTACTGCCCCAGTTA CTTCTATTGGCAACACAGACAGCCGATTCTTTACAAAC CTCACCACTGGCATCTACAGGTTCTACCCCATCTACATA CAGCCTGAAGACTTCAAACGCATCCATGGAGTCAACG AGAAAATCTCAGTCCAAGCCTATGAGACCCAAGTGAA ATTCATCTTTGAGTTGATTCAGAATGCTGACACAGACC AGGAGCCAGTTTCTCACCTGCACAAACTG NYU_E 69333677 69349911 InFrame 8323 ATGAGGGTAGCTGCGGCGACTGCGGCGGCTGGAGCG GGGCCGGCCATGGCGGTGTGGACGCGGGCCACCAAA GCGGGGCTGGTGGAGCTGCTCCTGAGGGAGCGCTGG GTCCGAGTGGTGGCCGAGCTGAGCGGGGAGAGCCTG AGCCTGACGGGCGACGCCGCCGCGGCCGAGCTGGAG CCCGCTCTGGGACCCGCGGCCGCCGCCTTCAACGGCCT CCCAAACGGCGGCGGCGCGGGCGACTCGCTGCCCGG GAGCCCAAgccgcggcctggggcccccgagcccgccggcgccgcct cggggccccgcgggtgaggcgggcgcgtcgccgcccgtgcccgggT GCGGGTGGTGAAGCAAGAGGCGGGCGGCCTGGGCAT CAGCATCAAGGGCGGCCGCGAGAACCGGATGCCGATC CTCATCTCCAAGATCTTCCCCGGGCTGGCTGCCGACCA GAGCCGGGCGCTGCGGCTGGGCGACGCCATCCTGTCG GTGAACGGCACCGACCTGCGCCAGGCCACCCACGACC AGGCCGTGCAGGCGCTGAAGCGCGCGGGCAAGGAGG TGCTGCTGGAGGTCAAGTTCATCCGAGAAGTAACACC ATATATCAAGAAGCCATCATTAGTATCAGATCTGCCGT GGGAAGGTGCAGCCCCCCAGTCACCAAGCTTTAGTGG CAGTGAGGACTCTGGTTCGCCAAAACACCAGAACAGC ACCAAGGACAGGAAGATCATCCCTCTCAAAATGTGCTT TGCTGCTAGAAACCTAAGCATGCCGGATCTGGAAAAC AGATTGATAGAGCTACATTCTCCTGATAGCAGGAACAC GTTGATCCTACGCTGCAAAGATACAGCCACAGCACACT CCTGGTTCGTAGCTATCCACACCAACATAATGGCTCTC CTCCCACAGGTGTTGGCTGAACTCAACGCCATGCTTGG GGCAACCAGTACAGCAGGAGGCAGTAAAGAGGTGAA GCATATTGCCTGGCTGGCAGAACAGGCAAAACTAGAT GGTGGAAGACAGCAATGGAGACCTGTCCTCATGGCTG TGACTGAGAAGGATTTGCTGCTCTATGACTGTATGCCG TGGACAAGAGATGCCTGGGCGTCACCATGCCACAGCT ACCCACTTGTTGCCACCAGGTTGGTTCATTCTGGCTCC GGATGTCGATCCCCCTCCCTTGGATCTGACCTTACATTT GCTACCAGGACAGGCTCTCGACAGGGCATTGAGATGC ATCTCTTCAGGGTGGAGACACATCGGGATCTGTCATCC TGGACCAGGATACTTGTTCAGGGTTGCCATGCTGCTGC TGAGCTGATCAAGGAAGTCTCTCTAGGCTGCATGTTAA ATGGCCAAGAGGTGAGGCTTACTATTCACTATGAAAAT GGGTTCACCATCTCAAGGGAAAATGGAGGCTCCAGCA GCATATTGTACCGCTACCCCTTTGAAAGGCTGAAGATG TCTGCTGATGATGGCATCCGAAATCTATACTTGGATTTT GGTGGTCCCGAGGGAGAACTG|AAAGCCATTGATCTG GTGACGAAAGCCACAGAGGAGGACAAAGCCAAGAAC TACGAGGAGGCGCTGCGGCTGTACCAGCATGCGGTGG AGTACTTCCTCCACGCTATCAAGTATGAGGCCCACAGC GACAAGGCCAAGGAGAGCATTCGAGCCAAGTGCGTG CAGTACCTAGACCGGGCCGAGAAGCTGAAGGATTATT TACGAAGCAAAGAGAAACACGGCAAGAAGCCAGTCA AAGAGAACCAGAGTGAGGGCAAGGGCAGTGACAGTG ACAGTGAAGGGGATAATCCGGAGAAAAAGAAACTGC AAGAACAGCTGATGGGTGCCGTCGTGATGGAGAAGCC CAACATACGGTGGAACGACGTGGCCGGGCTGGAGGG GGCCAAGGAGGCCCTCAAAGAAGCTGTCATTTTGCCA ATCAAATTCCCACACTTGTTCACAGGCAAGCGCACCCC CTGGCGGGGGATTCTGCTGTTCGGACCCCCTGGCACA GGGAAATCCTACCTGGCCAAAGCCGTGGCAACAGAGG CCAACAACTCCACCTTCTTCTCTGTGTCCTCCTCAGATC TGATGTCCAAGTGGCTGGGGGAGAGTGAAAAGCTGG TCAAGAACCTGTTTGAGCTGGCCAGGCAGCACAAGCC CTCCATCATCTTCATCGATGAGGTGGATTCCCTCTGCG GGTCCCGAAATGAAAATGAGAGTGAGGCCGCCCGGA GGATCAAAACGGAGTTCTTGGTCCAGATGCAGGGGGT GGGGAATAACAATGATGGGACTCTGGTTCTTGGAGCC ACAAACATCCCATGGGTGTTGGATTCGGCCATCAGGA GGAGGTTTGAAAAACGAATTTATATCCCCTTGCCGGAG GAAGCTGCCCGCGCCCAGATGTTCCGGTTGCATCTCGG GAGCACTCCCCACAACCTCACGGATGCAAACATCCACG AGCTGGCCCGGAAGACGGAAGGCTACTCGGGCGCGG ACATCAGCATCATCGTGCGGGACTCTCTCATGCAGCCC GTGAGGAAGGTGCAGTCGGCCACACACTTCAAAAAGG TCTGTGGCCCCTCTCGCACCAACCCCAGCATGATGATT GATGACCTCCTGACTCCATGCTCACCAGGGGACCCAG GAGCCATGGAGATGACTTGGATGGATGTCCCTGGGGA CAAACTCTTAGAGCCTGTGGTTTGCATGTCGGACATGC TGCGGTCTCTGGCCACCACCCGGCCCACGGTGAATGC AGACGACCTCCTGAAAGTGAAGAAATTCTCAGAGGAC TTTGGGCAAGAGAGT NYU_G 42759130 42744294 InFrame 8324 ATGAAGACCCCGGCGGACACAG|GTGACAGCGGGAA GGTGACCACAGTCGTAGCCACTCTAGGCCAAGGCCCA GAGCGCTCCCAAGAAGTGGCTTACACGGACATCAAAG TGATTGGCAATGGCTCATTTGGGGTCGTGTACCAGGC ACGGCTGGCAGAGACCAGGGAACTAGTCGCCATCAAG AAGGTTCTCCAGGACAAGAGGTTCAAGAACCGAGAGC TGCAGATCATGCGTAAGCTGGACCACTGCAATATTGTG AGGCTGAGATACTTTTTCTACTCCAGTGGCGAGAAGAA AGACGAGCTTTACCTAAATCTGGTGCTGGAATATGTGC CCGAGACAGTGTACCGGGTGGCCCGCCACTTCACCAA GGCCAAGTTGACCATCCCTATCCTCTATGTCAAGGTGT ACATGTACCAGCTCTTCCGCAGCTTGGCCTACATCCACT CCCAGGGCGTGTGTCACCGCGACATCAAGCCCCAGAA CCTGCTGGTGGACCCTGACACTGCTGTCCTCAAGCTCT GCGATTTTGGCAGTGCAAAGCAGTTGGTCCGAGGGGA GCCCAATGTCTCCTACATCTGTTCTCGCTACTACCGGGC CCCAGAGCTCATCTTTGGAGCCACTGATTACACCTCAT CCATCGATGTTTGGTCAGCTGGCTGTGTACTGGCAGAG CTCCTCTTGGGCCAGCCCATCTTCCCTGGGGACAGTGG GGTGGACCAGCTGGTGGAGATCATCAAGGTGCTGGG AACACCAACCCGGGAACAAATCCGAGAGATGAACCCC AACTACACGGAGTTCAAGTTCCCTCAGATTAAAGCTCA CCCCTGGACAAAGGTGTTCAAATCTCGAACGCCGCCA GAGGCCATCGCGCTCTGCTCTAGCCTGCTGGAGTACAC CCCATCCTCAAGGCTCTCCCCACTAGAGGCCTGTGCGC ACAGCTTCTTTGATGAACTGCGATGTCTGGGAACCCAG CTGCCTAACAACCGCCCACTTCCCCCTCTCTTCAACTTC AGTGCTGGTGAACTCTCCATCCAACCGTCTCTCAACGC CATTCTTATCCCTCCTCACTTGAGGTCCCCAGCGGGCAC TACCACCCTCACCCCGTCCTCACAAGCTTTAACTGAGAC TCCGACCAGCTCAGACTGGCAGTCGACCGATGCCACA CCTACCCTCACTAACTCCTCC NYU_B 6457893 6443410 InFrame 8325 ATGGGCATGGCCAGGGGCAGCCTCACTCGGGTTCCAG GGGTGATGGGAGAGGGCACTCAGGGCCCAGAGCTCA GCCTTGACCCTGACCCTTGCTCTCCCCAATCCACTCCGG GGCTCATGAAGGGGAACAAGCTGGAGGAGCAGGACC CTAGACCTCTGCAGCCCATACCAGGTCTCATGGAGGG GAACAAGCTGGAGGAGCAGGACTCTAGCCCTCCACAG TCCACTCCAGGGCTCATGAAGGGGAACAAGCGTGAGG AGCAGGGGCTGGGCCCCGAACCTGCGGCGCCCCAGCA GCCCACGGCGGAGGAGGAGGCCCTGATCGAGTTCCAC CGCTCCTACCGAGAGCTCTTCGAGTTCTTCTGCAACAA CACCACCATCCACGGCGCCATCCGCCTGGTGTGCTCCC AGCACAACCGCATGAAGACGGCCTTCTGGGCAGTGCT GTGGCTCTGCACCTTTGGCATGATGTACTGGCAATTCG GCCTGCTTTTCGGAGAGTACTTCAGCTACCCCGTCAGC CTCAACATCAACCTCAACTCGGACAAGCTCGTCTTCCCC GCAGTGACCATCTGCACCCTCAATCCCTACAGGTACCC GGAAATTAAAGAGGAGCTGGAGGAGCTGGACCGCAT CACAGAGCAGACGCTCTTTGACCTGTACAAATACAGCT CCTTCACCACTCTCGTGGCCGGCTCCCGCAGCCGTCGC GACCTGCGGGGGACTCTGCCGCACCCCTTGCAGCGCC TGAGGGTCCCGCCCCCGCCTCACGGGGCCCGTCGAGC CCGTAGCGTGGCCTCCAGCTTGCGGGACAACAACCCC CAGGTGGACTGGAAGGACTGGAAGATCGGCTTCCAGC TGTGCAACCAGAACAAATCGGACTGCTTCTACCAGACA TACTCATCAGGGGTGGATGCGGTGAGGGAGTGGTACC GCTTCCACTACATCAACATCCTGTCGAGGCTGCCAGAG ACTCTGCCATCCCTGGAGGAGGACACGCTGGGCAACT TCATCTTCGCCTGCCGCTTCAACCAGGTCTCCTGCAACC AGGCGAATTACTCTCACTTCCACCACCCGATGTATGGA AACTGCTATACTTTCAATGACAAGAACAACTCCAACCT CTGGATGTCTTCCATGCCTGGAATCAACAACGGTCTGT CCCTGATGCTGCGCGCAGAGCAGAATGACTTCATTCCC CTGCTGTCCACAGTGACTGGGGCCCGGGTAATGGTGC ACGGGCAGGATGAACCTGCCTTTATGGATGATGGTGG CTTTAACTTGCGGCCTGGCGTGGAGACCTCCATCAGCA TGAGGAAGGAAACCCTGGACAGACTTGGGGGCGATT ATGGCGACTGCACCAAGAATGGCAGTGATGTTCCTGTT GAGAACCTTTACCCTTCAAAGTACACACAGCAGGTGTG TATTCACTCCTGCTTCCAGGAGAGCATGATCAAGGAGT GTGGCTGTGCCTACATCTTCTATCCGCGGCCCCAGAAC GTGGAGTACTGTGACTACAGAAAGCACAGTTCCTGGG GGTACTGCTACTATAAGCTCCAGGTTGACTTCTCCTCA GACCACCTGGGCTGTTTCACCAAGTGCCGGAAGCCAT GCAGCGTGACCAGCTACCAGCTCTCTGCTGGTTACTCA CGATGGCCCTCGGTGACATCCCAGGAATGGGTCTTCCA GATGCTATCGCGACAGAACAATTACACCGTCAACAACA AGAGAAATGGAGTGGCCAAAGTCAACATCTTCTTCAA GGAGCTGAACTACAAAACCAATTCTGAGTCTCCCTCTG TCACG|GTGCTCCTGGAGCTGTTGGTGGGAATATACCC CTCAGGGGTTATTGGACTGGTCCCTCACCTAGGGGAC AGGGAGAAGAGAGATAGTGTGTGTCCCCAAGGAAAA TATATCCACCCTCAAAATAATTCGATTTGCTGTACCAAG TGCCACAAAGGAACCTACTTGTACAATGACTGTCCAGG CCCGGGGCAGGATACGGACTGCAGGGAGTGTGAGAG CGGCTCCTTCACCGCTTCAGAAAACCACCTCAGACACT GCCTCAGCTGCTCCAAATGCCGAAAGGAAATGGGTCA GGTGGAGATCTCTTCTTGCACAGTGGACCGGGACACC GTGTGTGGCTGCAGGAAGAACCAGTACCGGCATTATT GGAGTGAAAACCTTTTCCAGTGCTTCAATTGCAGCCTC TGCCTCAATGGGACCGTGCACCTCTCCTGCCAGGAGAA ACAGAACACCGTGTGCACCTGCCATGCAGGTTTCTTTC TAAGAGAAAACGAGTGTGTCTCCTGTAGTAACTGTAA GAAAAGCCTGGAGTGCACGAAGTTGTGCCTACCCCAG ATTGAGAATGTTAAGGGCACTGAGGACTCAGGCACCA CAGTGCTGTTGCCCCTGGTCATTTTCTTTGGTCTTTGCC TTTTATCCCTCCTCTTCATTGGTTTAATGTATCGCTACCA ACGGTGGAAGTCCAAGCTCTACTCCATTGTTTGTGGGA AATCGACACCTGAAAAAGAGGGGGAGCTTGAAGGAA CTACTACTAAGCccctggccccaaacccaagcttcagtcccactcc aggcttcacccccaccctgggcttcagtcccgtgcccagttccaccttca cctccagctccaCCTATACCCCCGGTGACTGTCCCAACTTT GCGGCTCCCCGCAGAGAGGTGGCACCACCCTATCAGG GGGCTGACCCCATCCTTGCGACAGCCCTCGCCTCCGAC CCCATCCCCAACCCCCTTCAGAAGTGGGAGGACAGCG CCCACAAGCCACAGAGCCTAGACACTGATGACCCCGC GACGCTGTACGCCGTGGTGGAGAACGTGCCCCCGTTG CGCTGGAAGGAATTCGTGCGGCGCCTAGGGCTGAGCG ACCACGAGATCGATCGGCTGGAGCTGCAGAACGGGC GCTGCCTGCGCGAGGCGCAATACAGCATGCTGGCGAC CTGGAGGCGGCGCACGCCGCGGCGCGAGGCCACGCT GGAGCTGCTGGGACGCGTGCTCCGCGACATGGACCTG CTGGGCTGCCTGGAGGACATCGAGGAGGCGCTTTgcgg ccccgccgccctcccgcccgcgcccAGTCTTCTCAGA G17675. 69230529 63195940 InFrame 8326 ATGGTGAGGAGCAGGCAAATGTGCAATACCAACATGT TCGA-19- CTGTACCTACTGATGGTGCTGTAACCACCTCACAGATT 2624- CCAGCTTCGGAACAAGAGACCCTGGTTAGACCAAAGC 01A-01R- CATTGCTTTTGAAGTTATTAAAGTCTGTTGGTGCACAA 1850- AAAGACACTTATACTATGAAAGAGGTTCTTTTTTATCTT 01.2 GGCCAGTATATTATGACTAAACGATTATATGATGAGAA GCAACAACATATTGTATATTGTTCAAATGATCTTCTAG GAGATTTGTTTGGCGTGCCAAGCTTCTCTGTGAAAGAG CACAGGAAAATATATACCATGATCTACAGGAACTTGGT AGTAGTCAATCAGCAGGAATCATCGGACTCAGGTACA TCTGTGAGTGAGAACAGGTGTCACCTTGAAGGTGGGA GTGATCAAAAGGACCTTGTACAAGAGCTTCAGGAAGA GAAACCTTCATCTTCACATTTGGTTTCTAGACCATCTAC CTCATCTAGAAGGAGAGCAATTAGTGAGACAGAAGAA AATTCAGATGAATTATCTGGTGAACGACAAAGAAAAC GCCACAAATCTGATAGTATTTCCCTTTCCTTTGATGAAA GCCTGGCTCTGTGTGTAATAAGGGAGATATGTTGTGA AAGAAGCAGTAGCAGTGAATCTACAGGGACGCCATCG AATCCGGATCTTGATGCTGGTGTAAGTGAACATTCAGG TGATTGGTTGGATCAGGATTCAGTTTCAGATCAGTTTA GTGTAGAATTTGAAGTTGAATCTCTCGACTCAGAAGAT TATAGCCTTAGTGAAGAAGGACAAGAACTCTCAGATG AAGATGATGAGGTATATCAAGTTACTGTGTATCAGGC AGGGGAGAGTGATACAGATTCATTTGAAGAAGATCCT GAAATTTCCTTAGCT|GAATCCGAGGGTGTTTCCTGCC ACTATTGGTCGCTGTTTGACGGGCACGCGGGGTCCGG GGCCGCGGTGGTGGCGTCACGCCTGCTGCAGCACCAC ATCACGGAGCAGCTGCAGGACATCGTGGACATCCTGA AGAACTCCGCCGTCCTGCCCCCTACCTGCCTGGGGGAG GAGCCTGAGAACACGCCCGCCAACAGCCGGACTCTGA CCCGGGCAGCCTCCCTGCGCGGAGGGGTGGGGGCCC CGGGCTCCCCCAGCACGCCCCCCACACGCTTCTTTACC GAGAAGAAGATTCCCCATGAGTGCCTGGTCATCGGAG CGCTTGAAAGTGCATTCAAGGAAATGGACCTACAGAT AGAACGAGAGAGGAGTTCATATAATATATCTGGTGGC TGCACGGCCCTCATTGTGATTTGCCTTTTGGGGAAGCT GTATGTTGCAAATGCTGGGGATAGCAGGGCCATAATC ATCAGAAATGGAGAAATTATCCCCATGTCTTCAGAATT TACCCCCGAGACGGAGCGCCAGCGACTTCAGTACCTG GCATTCATGCAGCCTCACTTGCTGGGAAATGAGTTCAC ACATTTGGAGTTTCCAAGGAGAGTACAGAGAAAGGAG CTTGGAAAGAAGATGCTCTACAGGGACTTTAATATGAC AGGCTGGGCATACAAAACCATTGAGGATGAGGACTTG AAGTTCCCCCTTATATATGGAGAAGGCAAGAAGGCCC GGGTAATGGCAACTATTGGAGTGACCAGGGGACTTGG GGACCATGACCTGAAGGTGCATGACTCCAACATCTACA TTAAACCATTCCTGTCTTCAGCTCCAGAGGTAAGAATC TACGATCTTTCAAAATATGATCATGGATCAGATGATGT GCTGATCTTGGCCACTGATGGACTCTGGGACGTTTTAT CAAATGAAGAAGTAGCAGAAGCAATCACTCAGTTTCTT CCTAACTGTGATCCAGATGATCCTCACAGGTACACACT GGCAGCTCAGGACCTGGTGATGCGTGCCCGGGGTGTG CTGAAGGACAGAGGATGGCGGATATCTAATGACCGAC TGGGCTCAGGAGACGACATTTCTGTATATGTCATTCCT TTAATACATGGAAACAAGCTGTCA G17484. 155385535 156384545 InFrame 8327 ATGGACCCTAGAAATACTGCTATGTTAGGATTGGGTTC TCGA-14- TGATTCCGAAGGTTTTTCAAGAAAGAGTCCTTCTGCCA 0787- TCAGTACTGGCACATTGGTCAGTAAGAGAGAAGTAGA 01A-01R- GCTAGAAAAAAACACAAAGGAGGAAGAGGACCTTCG 1849- CAAACGGAATCGAGAAAGAAACATCGAAGCTGGGAA 01.2 AGATGATGGTTTGACTGATGCACAGCAACAGTTTTCAG TGAAAGAAACAAACTTTTCAGAGGGAAATTTAAAATT GAAAATTGGCCTCCAGGCTAAGAGAACTAAAAAACCT CCAAAGAACTTGGAGAACTATGTATGTCGACCTGCCAT AAAAACAACTATTAAGCACCCAAGGAAAGCACTTAAA AGTGGAAAGATGACGGATGAAAAGAATGAACACTGTC CTTCAAAACGAGACCCTTCAAAGTTGTACAAGAAAGCA GATGATGTTGCAGCCATTGAATGCCAGTCTGAAGAAG TCATCCGTCTTCATTCACAGGGAGAAAACAATCCTTTG TCTAAGAAGCTGTCTCCAGTACACTCAGAAATGGCAGA TTATATTAATGCAACGCCATCTACTC-TTC-FTGGTAGCCG GGATCCTGATTTAAAGGACAGAGCATTACTTAATGGA GGAACTAGTGTAACAGAAAAGTTGGCACAGCTGATTG CTACCTGTCCTCCTTCCAAGTCTTCCAAGACAAAACCGA AGAAGTTAGGAACTGGCACTACAGCAGGATTGGTTAG CAAGGATTTGATCAGGAAAGCAGGTGTTGGCTCTGTA GCTGGAATAATACATAAGGACTTAATAAAAAAGCCAA CCATCAGCACAGCAGTTGGATTGGTAACTAAAGATCCT GGGAAAAAGCCAGTGTTTAATGCAGCAGTAGGATTGG TCAATAAGGACTCTGTGAAAAAACTGGGAACTGGCAC TACAGCGGTATTCATTAATAAAAACTTAGGCAAAAAGC CAGGAACTATCACTACAGTAGGACTGCTAAGCAAAGA TTCAGGAAAGAAGCTAGGAATTGGTATTGTTCCAGGTT TAGTGCATAAAGAGTCTGGCAAGAAGTTAGGACTTGG CACTGTGGTTGGACTGGTTAATAAAGATTTGGGAAAG AAATTGGGTTCTACTGTTGGCCTAGTGGCCAAGGACTG TGCAAAGAAGATTGTAGCAAGTTCAGCAATGGGATTG GTTAATAAGGACATTGGAAAGAAACTAATGAGTTGTC CTTTGGCAGGTCTGATCAGTAAAGATGCCATAAACCTT AAAGCCGAAGCACTGCTCCCCACTCAGGAACCGCTTAA GGCTTCTTGTAGTACAAACATCAATAATCAGGAAAGTC AGGAACTTTCTGAATCCCTGAAAGATAGTGCCACCAGC AAAACTTTTGAAAAGAATGTTGTACGGCAGAATAAAG AAAGCATATTGGAAAAGTTCTCAGTACGAAAAGAAAT CATTAATTTGGAGAAAGAAATGTTTAATGAAGGAACA TGCATTCAGCAAGACAGTTTCTCATCCAGTGAAAAGGG ATCTTATGAAACCTCAAAGCATGAAAAGCAGCCTCCTG TATATTGCACTTCTCCGGACTTTAAAATGGGAGGTGCT TCTGATGTATCTACCGCTAAATCCCCATTCAGTGCAGTA GGAGAAAGCAATCTCCCTTCCCCATCACCTACTGTATCT GTTAATCCTTTAACCAGAAGTCCCCCTGAAACTTCTTCA CAGTTGGCTCCTAATCCATTACTTTTAAGTTCTACTACA GAACTAATCGAAGAAATTTCTGAATCTGTTGGAAAGA ACCAGTTTACTTCTGAAAGTACCCACTTGAACGTTGGT CATAGGTCAGTTGGTCATAGTATAAGTATTGAATGTAA AGGGATTGATAAAGAGGTAAATGATTCAAAAACTACC CATATAGATATTCCAAGAATAAGCTCTTCCCTTGGAAA AAAGCCAAGTTTGACTTCTGAATCCAGCATTCATACTA TTACTCCTTCAGTTGTTAACTTCACTAGTTTATTTAGTA ATAAGCCTTTTTTAAAACTGGGTGCAGTATCTGCATCA GACAAACACTGCCAAGTTGCTGAAAGCCTAAGTACTA GTTTGCAGTCCAAACCATTAAAAAAAAGAAAAGGAAG AAAACCTCGGTGGACTAAAGTGGTGGCAAGAAGCACA TGCCGGTCTCCAAAAGGGCTAGAATTAGAAAGATCAG AGCTTTTTAAAAACGTTTCATGTAGCTCACTATCAAATA GTAATTCTGAGCCAGCCAAGTTTATGAAAAACATTGGA CCCCCTTCATTTGTAGATCATGACTTCCTTAAACGCCGA TTGCCAAAGTTGAGCAAATCCACAGCTCCATCTCTTGC TCTCTTAGCTGATAGTGAAAAACCATCTCATAAGTCTTT TGCTACTCACAAACTATCCTCCAGTATGTGTGTCTCTAG TGACCTTTTGTCTGATATTTATAAGCCCAAAAGAGGAA GGCCTAAATCTAAGGAGATGCCTCAACTGGAAGGGCC ACCTAAAAGGACTTTAAAAATCCCTGCTTCTAAAGTGT TTTCTTTACAGTCTAAGGAAGAACAAGAACCCCCAATT TTACAGCCAGAAATTGAAATCCCTTCCTTCAAACAAGG TCTGTCTGTGTCTCCTTTTCCAAAAAAGAGAGGCAGGC CTAAGAGGCAAATGAGGTCACCAGTCAAGATGAAGCC ACCTGTACTGTCAGTGGCTCCATTTGTTGCCACTGAAA GTCCAAGCAAGCTAGAATCTGAAAGTGACAACCATAG AAGTAGCAGTGATTTCTTTGAGAGCGAGGATCAACTTC AGGATCCAGATGACCTAGATGACAGTCATAGGCCAAG TGTCTGTAGTATGAGTGACCTTGAGATGGAACCAGAT AAAAAAATTACCAAGAGAAACAATGGACAATTAATGA AAACAATTATCCGCAAAATAAATAAAATGAAGACTTTA AAGAGAAAGAAACTGTTGAATCAGATTCTTTCAAGTTC TGTAGAATCAAGTAATAAAGGGAAAGTGCAATCCAAA CTCCATAATACGGTATCAAGTCTTGCTGCCACATTTGG CTCTAAATTGGGCCAACAGATAAATGTCAGCAAGAAA GGAACCATTTATATAGGAAAGAGAAGAGGTCGCAAAC CAAAAACTGTCTTAAATGGTATTCTTTCTGGTAGTCCTA CTAGCCTTGCTGTTCTTGAGCAAACAGCTCAACAGGCA GCTGGGTCAGCATTAGGACAGATTCTTCCCCCATTACT GCCTTCATCTGCTAGTAGTTCTGAGATTCTTCCATCACC TATTTGCTCTCAGTCTTCTGGGACTAGTGGAGGTCAGA GCCCTGTAAGTAGTGATGCAGGTTTTGTTGAACCCAGT TCAGTGCCATATTTGCATTTACACTCCAGACAGGGCAG TATGATTCAGACTCTTGCAATGAAGAAGGCCTCAAAG GGGAGGAGGCGGTTATCTCCTCCTACTTTGTTGCCAAA TTCTCCTTCGCACTTGAGTGAACTCACATCTCTAAAAGA AGCTACTCCTTCCCCAATCAGTGAGTCTCATAGTGATG AGACCATTCCCAGTGATAGTGGAATTGGAACAGATAA TAACAGCACATCAGACAGGGCAGAGAAATTTTGTGGG CAAAAAAAGAGGAGGCATTCTTTTGAGCATGTTTCTCT GATTCCCCCTGAAACCTCTACAGTGCTAAGCAGTCTTA AAGAAAAACATAAACACAAATGTAAGCGCAGGAATCA TGATTACCTCAGCTATGACAAGATGAAAAGGCAGAAA CGAAAACGGAAAAAGAAATATCCCCAGCTTCGAAATA GACAGGATCCAGACTTTATTGCAGAGCTGGAGGAACT AATAAGTCGCCTAAGTGAAATTCGGATCACTCATCGAA GTCATCATTTTATCCCCCGAGATCTTCTGCCAACTATCT TTCGAATCAACTTTAATAGTTTCTATACACATCCTTCTTT CCCCTTAGACCCTTTGCACTACATTCGAAAACCTGACTT AAAAAAGAAAAGAGGGAGACCCCCTAAGATGAGGGA GGCAATGGCTGAAATGCCTTTTATGCACAGCCTTAGTT TTCCTCTTTCTAGTACTGGATTCTATCCATCTTATGGTAT GCCTTACTCTCCTTCACCCCTTACAGCTGCTCCCATAGG ATTAGGTTACTATGGAAGGTATCCTCCCACTCTTTATCC ACCTCCTCCATCTCCTTCTTTCACCACGCCACTTCCACCT CCTTCCTATATGCATGCTGGTCATTTACTTCTCAATCCT GCCAAATACCATAAGAAAAAGCATAAGCTACTTCGACA GGAGGCCTTTCTTACAACCAGCAGGACTCCCCTCCTTT CCATGAGTACCTACCCCAGTGTTCCTCCTGAGATGGCC TATGGTTGGATGGTTGAGCACAAACACAGGCACCGTC ACAAACACAGAGAACACCGTTCTTCTGAACAACCCCAG GTTTCTATGGACACTGGCTCTTCCCGATCTGTCCTGGA ATCTTTGAAGCGCTATAGATTTGGAAAGGATGCTGTTG GAGAGCGATATAAGCATAAGGAAAAGCACCGTTGTCA CATGTCCTGCCCTCATCTCTCTCCTTCAAAAAGCTTAAT AAACAGAGAGGAACAGTGGGTCCACCGAGAGCCTTCA GAATCTAGTCCATTGGCCTTGGGATTGCAGACACCTTT ACAGATTGACTGTTCAGAAAGTTCTCCAAGCTTATCCC TTGGAGGATTCACTCCCAACTCTGAGCCAGCCAGCAGT GATGAACATACAAACCTTTTCACAAGTGCAATAGGCAG CTGCAGAGTTTCAAACCCTAACTCCAGTGGCCGGAAG AAATTAACTGACAGCCCTGGACTCTTTTCTGCACAGGA CACTTCACTAAATCGGCTTCACAGAAAGGAGTCACTGC CTTCTAACGAAAGGGCAGTACAGACTTTGGCAGGCTC CCAGCCAACCTCTGATAAACCCTCCCAGCGGCCATCAG AGAGCACAAATTGTAGCCCTACCCGGAAAAGGTCTTC ATCTGAGAGTACTTCTTCAACAGTAAACGGAGTTCCCT CTCGAAGTCCAAGATTAGTTGCTTCTGGGGATGACTCT GTGGATAGTCTGCTGCAGCGGATGGTACAAAATGAGG ACCAAGAGCCCATGGAGAAAAGTATTGATGCTGTGAT TGCAACTGCCTCTGCACCACCTTCTTCCAGTCCAGGCC GTAGCCACAGCAAGGACCGAACCCTGGGAAAACCAGA CAGCCTTTTAGTGCCTGCAGTCACAAGTGACTCTTGCA ATAATAGCATCTCACTCCTATCTGAAAAGTTGACAAGC AGCTGTTCCCCCCATCATATCAAGAGAAGTGTAGTGGA AGCTATGCAACGCCAAGCTCGGAAAATGTGCAATTAC GACAAAATCTTGGCCACAAAGAAAAACCTAGACCATG TCAATAAAATCTTAAAAGCCAAAAAACTTCAAAGGCAG GCCAGGACAGGGAATAACTTTGTGAAACGTAGGCCAG GTCGACCTCGGAAATGTCCCCTTCAGGCTGTCGTATCA ATGCAAGCATTCCAGGCTGCTCAGTTTGTCAACCCAGA ATTGAACAGAGACGAGGAAGGAGCAGCACTGCACCTC AGTCCTGACACAGTTACAGATGTAATTGAGGCTGTTGT TCAGAGTGTAAATCTGAACCCAGAACATAAAAAGGGG TTGAAGAGAAAAGGTTGGCTATTGGAAGAACAGACCA GAAAAAAGCAGAAGCCATTACCAGAGGAAGAAGAGC AAGAGAATAATAAAAGCTTTAATGAAGCACCAGTTGA GATTCCCAGTCCTTCTGAAACCCCAGCTAAACCTTCTGA ACCTGAAAGTACCTTGCAGCCTGTGCTTTCTCTCATCCC AAGGGAAAAGAAGCCCCCACGTCCCCCAAAGAAGAAG TATCAGAAAGCAGGGCTGTATTCTGACGTTTACAAAAC TACAGA|CTTCTCACCTGGGGCGGGTGGGTTCTGCACC ACCCTCCCACCCTCCTTCCTCCGTGTGGACGATAGAGC CACATCCAGCACCACGGACAGCTCCCGGGCGCCTTCAT CTCCTCGTCCTCCAGGCAGCACAAGCCATTGTGGAATC TCCACCAGGTGTACAGAACGGTGCCTCTGCGTCCTGCC ACTCAGGACCTCTCAAGTCCCCGATGTGATGGCTCCTC AGCATGATCAGGAgaaattccatgatcttgcttattcctgtcttggg aagtccttctccatgtctaaccaagatctatatggctatagcaccagctc tttggctcttggcttggcatggctaagttgggagACCAAAAAGAAG AATGTACTTCATCTGGTTGGGCTGGATTCCCTC G17792. 100065175 10061309 InFrame 8328 ATGAGCGGGGGCAAGAAGAAGAGTAGTTTCCAAATCA TCGA-28- CCAGCGTCACCACGGACTATGAGGGCCCTGGGAGCCC 5204- AGGGGCTTCGGATCCCCCTACCCCACAGCCCCCAACCG 01A-01R- GGCCCCCGCCCCGCCTGCCCAATGGGGAGCCCAGCCC 1850- CGATCCGGGGGGCAAGGGCACCCCCCGGAATGGCTCC 01.4 CCACCACCTGGGGCCCCTTCCTCCCGTTTCCGGGTGGT GAAGCTGCCCCACGGCCTGGGAGAGCCTTATCGCCGC GGTCGCTGGACGTGTGTGGATGTTTATGAGCGAGACC TGGAGCCCCACAGCTTCGGCGGACTCCTGGAGGGAAT TCGAGGGGCCTCAGGGGGCGCCGGGGGCAGATCTTT GGATTCCAGGTTGGAGCTGGCCAGCCTCGGCCTGGGC GCCCCCACCCCACCGTCAGGCCTGTCTCAGGGCCCCAC CTCCTGGCTCCGTCCACCCCCCACCTCTCCTGGACCTCA GGCCCGCTCCTTCACTGGGGGACTGGGCCAGCTGGTG GTGCCCAGCAAAGCCAAGGCAGAGAAACCCCCACTGT CGGCCTCCTCACCCCAGCAGCGCCCCCCAGAGCCTGAG ACCGGTGAGAGTGCGGGCACATCCCGGGCTGCCACGC CCCTGCCCTCTCTGAGGGTGGAAGCGGAGGCTGGGGG CTCAGGGGCCAGGACCCCTCCACTGTCCCGGAGGAAA GCTGTAGACATGCGGCTGCGGATGGAGTTGGGTGCTC CAGAAGAGATGGGGCAGGTGCCCCCACTTGACTCTCG CCCCAGCTCCCCAGCCCTCTACTTCACCCACGATGCCA GCCTGGTTCACAAATCTCCAGACCCCTTCGGAGCAGTA GCAGCTCAGAAGTTCAGCCTGGCCCACTCCATGTTGGC CATCAGTGGTCACCTAGACAGCGACGATGATAGTGGC TCCGGAAGCCTGGTTGGCATTGACAACAAAATCGAGC AAGCCATG|TGTTTTCTTCTGGAGGCAAAAAATTAAACC AACCATCTCAGGACACCCTGACTCCAAGAAACACTCAT TGAAGAAGATGGAGAAGACTCTCCAGGTGGTTGAGAC TTTGAGGTTGGTCGAGCTCCCAAAAGAGGCTAAGCCC AAGTTGGGTGAGTCCCCCGAGCTGGCAGATCCCTGCG TGTTGGCCAAGACTACAGAGGAGACCGAGGTGGAGCT GGGCCAACAGGGCCAATCCCTACTGCAGCTGCCGAGG ACGGCCGTCAAGTCTGTCTCCACGCTCATGGTCTCTGC CCTGCAGAGCGGCTGGCAGATGTGCAGCTGGAAGTCA TCAGTGAGTTCTGCCTCAGTCAGCTCCCAAGTGAGGAC GCAGTCACCTTTGAAGACTCCGGAGGCTGAGTTGCTGT GGGAGGTGTACCTGGTGCTGTGGGCCGTTCGGAAACA CCTGCGCCGGCTGTACCGCAGGCAGGAGAGGCACAG ACGGCACCACGTCCGATGCCATGCTGCCCCCCGACCCA ACCCGGCTCAGTCCCTGAAACTGGATGCCCAAAGTCCC CTC BT299 23037536 1256473 InFrame 8329 ATGGCTCTGCGGAGGCTGGGGGCCGCGCTGCTGCTGC TGCCGCTGCTCGCCGCCGTGGAAg|GGGCCGGCCAGG ACGTGGGCCGAAGCTGCATCCTGGTCTCCATTGCGGG CAAGAATGTCATGCTGGACTGTGGAATGCACATGGGC TTCAATGACGACCGACGCTTCCCTGACTTCTCCTACATC ACCCAGAACGGCCGCCTAACAGACTTCCTGGACTGTGT GATCATTAGCCACTTCCACCTGGACCACTGCGGGGCAC TCCCCTACTTCAGCGAGATGGTGGGCTACGACGGGCC CATCTACATGACTCACCCCACCCAGGCCATCTGCCCCAT CTTGCTGGAGGACTACCGCAAGATCGCCGTAGACAAG AAGGGCGAGGCCAACTTCTTCACCTCCCAGATGATCAA AGACTGCATGAAGAAGGTGGTGGCTGTCCACCTCCAC CAGACGGTCCAGGTAGATGATGAGCTGGAGATCAAG GCCTACTATGCAGGCCACGTGCTGGGGGCAGCCATGT TCCAGATTAAAGTGGGCTCAGAGTCTGTGGTCTACACG GGTGATTATAACATGACCCCAGACCGACACTTAGGAG CTGCCTGGATTGACAAGTGCCGCCCCAACCTGCTCATC ACAGAGTCCACGTACGCCACGACCATCCGTGACTCCAA GCGCTGCCGGGAGCGAGACTTCCTGAAGAAAGTCCAC GAGACCGTGGAGCGTGGTGGGAAGGTGCTGATACCT GTGTTCGCGCTGGGCCGCGCCCAGGAGCTCTGCATCC TCCTGGAGACCTTCTGGGAGCGCATGAACCTGAAGGT GCCCATCTACTTCTCCACGGGGCTGACCGAGAAGGCC AACCACTACTACAAGCTGTTCATCCCCTGGACCAACCA GAAGATCCGCAAGACTTTCGTGCAGAGGAACATGTTT GAGTTCAAGCACATCAAGGCCTTCGACCGGGCTTTTGC TGACAACCCAGGACCGATGGTTGTGTTTGCCACGCCA GGAATGCTGCACGCTGGGCAGTCCCTGCAGATCTTCC GGAAATGGGCCGGAAACGAAAAGAACATGGTCATCAT GCCCGGCTACTGCGTGCAGGGCACCGTCGGCCACAAG ATCCTCAGCGGGCAGCGGAAGCTCGAGATGGAGGGG CGGCAGGTGCTGGAGGTCAAGATGCAGGTGGAGTAC ATGTCATTCAGCGCACACGCGGACGCCAAGGGCATCA TGCAGCTGGTGGGCCAGGCAGAGCCGGAGAGCGTGC TGCTGGTGCATGGCGAGGCCAAGAAGATGGAGTTCCT GAAGCAGAAGATCGAGCAGGAGCTCCGGGTCAACTG CTACATGCCGGCCAATGGCGAGACGGTGACGCTGCCC ACAAGCCCCAGCATCCCCGTAGGCATCTCGCTGGGGCT GCTGAAGCGGGAGATGGCGCAGGGGCTGCTCCCTGA GGCCAAGAAGCCTCGGCTCCTGCACGGCACCCTGATC ATGAAGGACAGCAACTTCCGGCTGGTGTCCTCAGAGC AAGCCCTCAAAGAGCTGGGTCTGGCTGAGCACCAGCT GCGCTTCACCTGCCGCGTGCACCTGCATGACACACGCA AGGAGCAGGAGACGGCATTGCGCGTCTACAGCCACCT CAAGAGCGTCCTGAAGGACCACTGTGTGCAGCACCTC CCAGACGGCTCTGTGACTGTGGAGTCCGTCCTCCTCCA GGCCGCCGCCCCTTCTGAGGACCCAGGCACCAAGGTG CTGCTGGTCTCCTGGACCTACCAGGACGAGGAGCTGG GGAGCTTCCTCACATCTCTGCTGAAGAAGGGCCTCCCC CAGGCCCCCAGC G17667. 54373484 53494330 InFrame 8330 ATGAACCAGCCAGAGTCTGCCAACGATCCTGAACCCCT TCGA-26- GTGTGCAGTGTGTGGCCAAGCCCACTCCTTGGAGGAA 5134- AACCACTTCTACAGCTATCCAGAGGAAGTGGATGATG 01A-01R- ACCTCATCTGCCACATCTGCCTGCAGGCTTTGCTGGAC 1850- CCCCTGGACACTCCGTGTGGACACACCTACTGCACCCT 01.2 CTGCCTCACCAACTTCCTGGTGGAGAAGGACTTCTGTC CCATGGACCGCAAGCCTCTGGTTCTGCAGCACTGCAAG AAGTCCAGCATCCTGGTCAACAAACTCCTCAACAAGCT ACTGGTGACCTGCCCATTCAGGGAGCACTGCACCCAG GTGTTGCAGCGCTGTGACCTCGAGCATCACTTTCAAAC CAGCTGTAAAGGTGCCTCCCACTACGGCCTGACCAAA GATAGGAAGAGGCGCTCACAAGATGGCTGTCCAGACG GCTGTGCGAGCCTCACAGCCACGGCTCCCTCCCCAGAG GTTTCTGCAGCTGCCACCATCTCCTTAATGACAGACGA GCCTGGCCTAGACAACCCTGCCTACGTGTCCTCGGCAG AGGACGGGCAGCCAGCAATCAGCCCAGTGGACTCTGG CCGGAGCAACCGAACTAGGGCACGGCCCTTTGAGAGA TCCACTATTAGAAGCAGATCATTTAAAAAAATAAATCG AGCTTTGAGTGTTCTTCGAAGGACAAAGAGCGGGAGT GCAGTTGCCAACCATGCCGACCAGGGCAGGGAAAATT CTGAAAACACCACTGCCCCTGAAG|TTTGGAAACACAT GCTACTG GBM- 41198856 41192900 InFrame 8331 ATGTGGCTGAAGGTGGGGGGCCTACTTCGGGGGACC CUMC3338_L1 GGTGGACAGCTGGGCCAGACTGTTGGTTGGCCTTGTG GGGCCCTGGGGCCTGGGCCCCACCGCTGGGGACCATG TGGAGGTTCTTGGGCCCAAAAGTTTTACCAGGATGGG CCTGGGAGAGGCCTGGGTGAGGAGGACATTCGCAGG GCACGGGAGGCCCGTCCCAGGAAGACACCCCGGCCCC AGCTGAGTGACCGCTCTCGAGAACGCAAGGTGCCTGC CTCCCGCATCAGCCGCTTGGCCAACTTTGGGGGACTGG CTGTGGGCTTGGGGCTAGGAGTACTGGCCGAGATGGC TAAGAAGTCCATGCCAGGAGGTCGTCTGCAGTCAGAG GGTGGTTCTGGGCTGGACTCCAGCCCCTTCCTGTCGGA GGCCAATGCCGAGCGGATTGTGCAGACCTTATGTACA GTTCGAGGGGCCGCCCTCAAGGTTGGCCAGATGCTCA GCATCCAGGACAACAGCTTCATCAGCCCTCAGCTGCAG CACATCTTTGAGCGGGTCCGCCAGAGCGCCGACTTCAT GCCCCGCTGGCAGATGCTGagagttcttgaagaggagctcggc agggactggcaggccaaggtggcctccttggaggaggtgccctttgCC GCTGCCTCAATTGGGCAGGTGCACCAGGGCCTGCTGA GGGACGGGACGGAGGTGGCCGTGAAGATCCAGTACC CCGGCATAGCCCAGAGCATTCAGAGCGATGTCCAGAA CCTGCTGGCGGTACTCAAGATGAGCGCGGCCCTGCCC GCGGGCCTGTTTGCCGAGCAGAGCCTGCAGGCCTTGC AGCAGGAGCTGGCTTGGGAGTGTGACTACCGTCGTGA GGCGGCTTGTGCCCAGAATTTCAGGCAGCTGCTGGCA AATGACCCCTTCTTCCGGGTCCCAGCCGTGGTTAAGGA GCTGTGCACGACACGGGTGCTGGGCATGGAGCTGGCT GGAGGGGTCCCCCTGGACCAGTGCCAGGGCCTAAGCC AGGACCTGCGGAACCAGATTTGCTTCCAGCTCCTGACG CTGTGTCTGCGGGAGCTGTTTGAGTTCCGATTCATGCA GACTGACCCCAACTGGGCCAACTTCCTGTATGATGCCT CCAGCCACCAGGTGACCCTGCTGGACTTTGGTGCAAG CCGGGAGTTTGGGACAGAGTTCACAGACCATTACATC GAGGTGGTGAAGGCTGCAGCTGATGGAGACAGAGAC TGTGTCCTGCAGAAGTCCAGGGACCTCAAATTCCTCAC AGGCTTTGAAACCAAG|GGCGGACCCCGGAGGCCTGA GCGGCACCTGCCCCCAGCCCCCTGTGGGGCCCCGGGG CCCCCAGAAACCTGCAGGACGGAGCCAGACGGGGCG GGCACCATGAACAAGTTACGGCAGAGCCTGCGGCGGA GGAAGCCAGCCTACGTGCCCGAGGCGTCGCGCCCGCA CCAGTGGCAGGCAGACGAGGACGCGGTGCGGAAGGG CACGTGCAGCTTCCCGGTCAGGTACCTGGGTCACGTG GAGGTAGAGGAGTCCCGGGGAATGCACGTGTGTGAA GATGCGGTGAAGAAGCTGAAGGCGATGGGCCGAAAG TCCGTGAAGTCTGTCCTGTGGGTGTCAGCCGATGGGC TCCGAGTGGTGGACGACAAAACCAAGGATCTTCTGGT CGACCAGACCATCGAAAAGGTCTCCTTTTGTGCTCCTG ACCGCAACCTGGACAAGGCTTTCTCCTATATCTGTCGT GACGGGACTACCCGCCGCTGGATCTGCCACTGTTTTCT GGCACTGAAGGACTCCGGCGAGAGGCTGAGCCACGCT GTGGGCTGTGCTTTTGCCGCCTGCCTGGAGCGAAAAC AGCGACGGGAGAAGGAATGTGGGGTCACGGCCGCCT TCGATGCCAGCCGCACCAGCTTCGCCCGCGAGGGCTC CTTCCGCCTGTCTGGGGGTGGGCGGCCTGCTGAGCGA GAGGCCCCGGACAAGAAGAAAGCAGAGGCAGCAGCT GCCCCCACTGTGGCTCCTGGCCCTGCCCAGCCTGGGCA CGTGTCCCCGACACCAGCCACCACATCCCCTGGTGAGA AGGGTGAGGCAGGCACCCCTGTGGCTGCAGGCACCAC TGCGGCCGCCATCCCCCGGCGCCATGCACCCCTGGAG CAGCTGGTTCGCCAGGGCTCCTTCCGTGGGTTCCCAGC ACTCAGCCAGAAGAACTCGCCTTTCAAACGGCAGCTG AGCCTACGGCTGAATGAGCTGCCATCCACGCTGCAGC GCCGCACTGACTTCCAGGTGAAGGGCACAGTGCCTGA GATGGAGCCTCCTGGTGCCGGCGACAGTGACAGCATC AACGCTCTGTGCACACAGATCAGTTCATCTTTTGCCAG TGCTGGAGCGCCAGCACCAGGGCCACCACCTGCCACA ACAGGGACTTCTGCCTGGGGTGAGCCCTCCGTGCCCCC TGCAGCTGCCTTCCAGCCTGGGCACAAGCGGACACCTT CAGAGGCTGAGCGATGGCTGGAGGAGGTGTCACAGG TGGCCAAGGCCcagcagcagcagcagcagcaacagcaacagca gcagcagcagcagcagcaacagcagcaagcagcCTCAGTGGCCC CAGTGCCCACCATGCCTCCTGCCCTGCAGCCTTTCCCCG CCCCCGTGGGGCCCTTTGACGCTGCACCTGCCCAAGTG GCCGTGTTCCTGCCACCCCCACACATGCAGCCCCCTTTT GTGCCCGCCTACCCGGGCTTGGGCTACCCACCGATGCC CCGGGTGCCCGTGGTGGGCATCACACCCTCACAGATG GTGGCAAACGCCTTCTGCTCAGCCGCCCAGCTCCAGCC TCAGCCTGCCACTCTGCTTGGGAAAGCTGGGGCCTTCC CGCCCCCTGCCATACCCAGTGCCCCTGGGAGCCAGGCC CGCCCTCGCCCCAATGGGGCCCCCTGGCCCCCTGAGCC AGCGCCTGCCCCAGCTCCAGAGTTGGACCCCTTTGAGG CCCAGTGGGCGGCATTAGAAGGCAAAGCCACTGTAGA GAAACCCTCCAACCCCTTTTCTGGCGACCTGCAAAAGA CATTCGAGATTGAACTG G17815. 154918048 154904891 InFrame 8332 ATGGCCTCCTGCCCAGACTCTGATAATAGCTGGGTGCT TCGA-19- TGCTGGCTCCGAGAGCCTGCCAGTGGAGACACTGGGC 5960- CCGGCATCCAGGATGGACCCAGAATCTGAGAGAGCCC 01A-11R- TGCAGGCCCCTCACAGCCCCTCCAAGACAGATGGGAA 1850- AGAATTAGCTGGGACCATGGATGGAGAAGGGACGCT 01.4 CTTCCAGACTGAAAGCCCTCAGTCTGGCAGCATTCTAA CAGAGGAGACTGAGGTCAAGGGCACCCTGGAAGGTG ATGTTTGTGGTGTGGAGCCTCCTGGCCCAGGAGACAC AGTAGTCCAGGGAGACCTGCAGGAGACCACCGTGGTG ACAGGCCTGGGACCAGACACACAGGACCTGGAAGGC CAGAGCCCTCCACAGAGCCTGCCTTCAACCCCCAAAGC AGCTTGGATCAGGGAGGAGGGCCGCTGCTCCAGCAGT GACGATGACACCGACGTGGACATGGAGGGTCTGCGG AGACGGCGGGGCCGGGAGGCCGGCCCACCTCAGCCC ATGGTGCCCCTGGCTGTGGAGAACCAGGCTGGGGGTG AGGGTGCAGGCGGGGAGCTGGGCATCTCCCTCAACAT GTGCCTCCTTGGGGCCCTGGTTCTGCTTGGCCTGGGG GTCCTCCTCTTCTCAGGTGGCCTCTCAGAGTCTGAGAC TGGGCCCATGGAGGAAGTGGAGCGGCAGGTCCTCCCA GACCCCGAGGTGCTGGAAGCTGTGGGGGACAGGCAG GATGGGCTAAGGGAACAGCTGCAGGCCCCAGTGCCTC CTGACAGTGTCCCCAGCCTGCAAAACATGGGTCTTCTG CTGGACAAGCTGGCCAAGGAGAACCAGGACATCCGGC TGCTGCAGGCCCAGCTGCAGGCCCAAAAGGAAGAGCT TCAGAGCCTGATGCACCAGCCCAAAGGGCTAGAGGAG GAGAATGCCCAGCTCCGGGGGGCTCTGCAGCAGGGC GAAGCCTTCCAGCGGGCTCTGGAGTCAGAGCTGCAGC AGCTGCGGGCCCGGCTCCAGGGGCTGGAGGCCGACT GTGTCCGGGGCCCAGATGGGGTGTGCCTCAGTGGGG GTAGAGGCCCACAGGGTGACAAGGCCATCAGGGAGC AAGGCCCCAGGGAGCAGGAGCCAGAACTCAGCTTCCT GAAGCAGAAGGAACAGCTGGAGGCTGAGGCACAGGC ATTAAGGCAAGAGTTAGAGAGGCAGCGACGGCTGCT GGGGTCTGTACAGCAGGATCTGGAGAGGAGCTTGCA GGATGCCAGCCGCGGGGACCCAGCTCATGCTGGCTTG GCTGAGCTGGGCCACAGATTGGCCCAGAAACTGCAGG GCCTGGAGAACTGGGGCCAGGACCCTGGGGTCTCTGC CAATGCCTCAAAGGCCTGGCACCAGAAGTCCCACTTCC AGAATTCTAGGGAGTGGAGTGGAAAGGAAAAGTGGT GGGATGGGCAGAGAGACCGGAAGGCTGAGCACTGGA AACATAAGAAGGAAGAATCTGGCCGGGAAAGGAAGA AGAACTGGGGAGGTCAGGAGGACAGGGAGCCAGCAG GAAGGTGGAAGGAGGGCAGGCCAAGGGTGGAGGAG TCGGGGAGCAAGAAGGAGGGCAAGCGACAGGGCCCG AAGGAACCCCCAAGGAAAAGTGGTAGCTTCCACTCCT CTGGAGAAAAGCAGAAGCAACCTCGGTGGAGGGAAG GGACTAAGGACAGCCATGACCCCCTGCCATCCTGGGC AGAGCTGTTGAGGCCCAAGTACCGGGCACCCCAGGGC TGCTCAGGTGTGGACGAGTGTGCCCGGCAGGAGGGC CTGACTTTCTTTGGCACAGAGCTAGCCCCAGTGCGGCA ACAGGAGCTGGCCTCTCTGCTAAGAACATACTTGGCAC GGCTGCCCTGGGCTGGGCAGCTGACCAAGGAGCTACC CCTCTCACCTGCTTTCTTTGGTGAGGATGGCATCTTCCG TCATGACCGCCTCCGCTTCCGGGATTTTGTGGATGCCC TGGAGGACAGCTTGGAGGAGGTGGCTGTGCAACAGA CAGGTGATGATGATGAAGTAGATGACTTTGAGGACTT CATCTTCAGCCACTTCTTTGGAGACAAAGCACTGAAGA AGAG|ACTTGGAGCTGATGTCTGTGCTGTCCTCCGGCT CTCTGGTCCACTCAAGGAACAGTATGCTCAGGAGCAT GGCTTGAACTTCCAGAGACTCCTGGACACCAGCACCTA CAAGGAGGCCTTTCGGAAGGACATGATCCGCTGGGGA GAGGAGAAACGCCAGGCTGACCCAGGCTTCTTTTGCA GGAAGATTGTGGAGGGCATCTCCCAGCCCATCTGGCT GGTGAGTGACACACGGAGAGTGTCTGACATCCAGTGG TTTCGGGAGGCCTATGGGGCCGTGACGCAGACGGTCC GCGTTGTAGCGTTGGAGCAGAGCCGACAGCAGCGGG GCTGGGTGTTCACGCCAGGGGTGGACGATGCTGAGTC AGAATGTGGCCTGGACAACTTCGGGGACTTTGACTGG GTCATCGAGAACCATGGAGTTGAACAGCGCCTGGAGG AGCAGTTGGAGAACCTGATAGAATTTATCCGCTCCAGA CTT G17662. 58758160 50285014 InFrame 8333 ATGGAAGCACGTTCTATGCTGGTTCCACCCCAGGCATC TCGA-32- TGTGTGCTTCGAGGATGTGGCTATGGCATTCACACAG 1970- GAGGAGTGGGAACAGCTGGACCTGGCCCAGAGGACA 01A-01R- CTGTACCGAGAGGTGACACTGGAGACCTGGGAGCATA 1850- TTGTCTCCCTGGGGCTTTTCCTTTCCAAATCTGATGTGA 01.2 TCTCTCAGCTGGAGCAAGAAGAGGACCTGTGCAGGGC AGAGCAGGAGGCCCCCCGAG|GTAAGAGCAAAGAGG CGGAAATTAAGAGAATCAACAAGGAACTGGCCAACAT CCGCTCCAAGTTCAAAGGAGACAAAGCCTTGGATGGC TACAGTAAGAAAAAATATGTGTGTAAACTGCTTTTCAT CTTCCTGCTTGGCCATGACATTGACTTTGGGCACATGG AGGCTGTGAATCTGTTGAGTTCCAATAAATACACAGAG AAGCAAATAGGTTACCTGTTCATTTCTGTGCTGGTGAA CTCGAACTCGGAGCTGATCCGCCTCATCAACAACGCCA TCAAGAATGACCTGGCCAGCCGCAACCCCACCTTCATG TGCCTGGCCCTGCACTGCATCGCCAACGTGGGCAGCC GGGAGATGGGCGAGGCCTTTGCCGCTGACATCCCCCG CATCCTGGTGGCCGGGGACAGCATGGACAGTGTCAAG CAGAGTGCGGCCCTGTGCCTCCTTCGACTGTACAAGGC CTCGCCTGACCTGGTGCCCATGGGCGAGTGGACGGCG CGTGTGGTACACCTGCTCAATGACCAGCACATGGGTGT GGTCACGGCCGCCGTCAGCCTCATCACCTGTCTCTGCA AGAAGAACCCAGATGACTTCAAGACGTGCGTCTCTCTG GCTGTGTCGCGCCTGAGCCGGATCGTCTCCTCTGCCTC CACCGACCTCCAGGACTACACCTACTACTTCGTCCCAG CACCCTGGCTCTCGGTGAAGCTCCTGCGGCTGCTGCAG TGCTACCCGCCTCCAGAGGATGCGGCTGTGAAGGGGC GGCTGGTGGAATGTCTGGAGACTGTGCTCAACAAGGC CCAGGAGCCCCCCAAATCCAAGAAGGTGCAGCATTCC AACGCCAAGAACGCCATCCTCTTCGAGACCATCAGCCT CATCATCCACTATGACAGTGAGCCCAACCTCCTGGTTC GGGCCTGCAACCAGCTGGGCCAGTTCCTGCAGCACCG GGAGACCAACCTGCGCTACCTGGCCCTGGAGAGCATG TGCACGCTGGCCAGCTCCGAGTTCTCCCATGAAGCCGT CAAGACGCACATTGACACCGTCATCAATGCCCTCAAGA CGGAGCGGGACGTCAGCGTGCGGCAGCGGGCGGCTG ACCTCCTCTACGCCATGTGTGACCGGAGCAATGCCAAG CAGATCGTGTCGGAGATGCTGCGGTACCTGGAGACGG CAGACTACGCCATCCGCGAGGAGATCGTCCTGAAGGT GGCCATCCTGGCCGAGAAGTACGCCGTGGACTACAGC TGGTACGTGGACACCATCCTCAACCTCATCCGCATTGC GGGCGACTACGTGAGTGAGGAGGTGTGGTACCGTGT GCTACAGATCGTCACCAACCGTGATGACGTCCAGGGC TATGCCGCCAAGACCGTCTTTGAGGCGCTCCAGGCCCC TGCCTGTCACGAGAACATGGTGAAGGTTGGCGGCTAC ATCCTTGGGGAGTTTGGGAACCTGATTGCTGGGGACC CCCGCTCCAGCCCCCCAGTGCAGTTCTCCCTGCTCCACT CCAAGTTCCATCTGTGCAGCGTGGCCACGCGGGCGCT GCTGCTGTCCACCTACATCAAGTTCATCAACCTCTTCCC CGAGACCAAGGCCACCATCCAGGGCGTCCTGCGGGCC GGCTCCCAGCTGCGCAATGCTGACGTGGAGCTGCAGC AGCGAGCCGTGGAGTACCTCACCCTCAGCTCAGTGGC CAGCACCGACGTCCTGGCCACGGTGCTGGAGGAGATG CCGCCCTTCCCCGAGCGCGAGTCGTCCATCCTGGCCAA GCTGAAACGCAAGAAGGGGCCAGGGGCCGGCAGCGC CCTGGACGATGGCCGGAGGGACCCCAGCAGCAACGA CATCAACGGGGGCATGGAGCCCACCCCCAGCACTGTG TCGACGCCCTCGCCCTCCGCCGACCTCCTGGGGCTGCG GGCAGCCCCTCCCCCGGCAGCACCCCCGGCTTCTGCAG GAGCAGGGAACCTTCTGGTGGACGTCTTCGATGGCCC GGCCGCCCAGCCCAGCCTGGGGCCCACCCCCGAGGAG GCCTTCCTCAGCGAGCTGGAGCCGCCTGCCCCCGAGA GCCCCATGGCTTTGCTGGCTGACCCAGCTCCAGCTGCT GACCCAGGTCCTGAGGACATCGGCCCTCCCATTCCGGA AGCCGATGAGTTGCTGAATAAGTTTGTGTGTAAGAAC AACGGGGTCCTGTTCGAGAACCAGCTGCTGCAGATCG GAGTCAAGTCAGAGTTCCGACAGAACCTGGGCCGCAT GTATCTCTTCTATGGCAACAAGACCTCGGTGCAGTTCC AGAATTTCTCACCCACTGTGGTTCACCCGGGAGACCTC CAGACTCATCTGGCTGTGCAGACCAAGCGCGTGGCGG CGCAGGTGGACGGCGGCGCGCAGGTGCAGCAGGTGC TCAATATCGAGTGCCTGCGGGACTTCCTGACGCCCCCG CTGCTGTCCGTGCGCTTCCGGTACGGTGGCGCCCCCCA GGCCCTCACCCTGAAGCTCCCAGTGACCATCAACAAGT TCTTCCAGCCCACCGAGATGGCGGCCCAGGATTTCTTC CAGCGCTGGAAGCAGCTGAGCCTCCCTCAACAGGAGG CGCAGAAAATCTTCAAAGCCAACCACCCCATGGACGCA GAAGTTACTAAGGCCAAGCTTCTGGGGTTTGGCTCTGC TCTCCTGGACAATGTGGACCCCAACCCTGAGAACTTCG TGGGGGCGGGGATCATCCAGACTAAAGCCCTGCAGGT GGGCTGTCTGCTTCGGCTGGAGCCCAATGCCCAGGCC CAGATGTACCGGCTGACCCTGCGCACCAGCAAGGAGC CCGTCTCCCGTCACCTGTGTGAGCTGCTGGCACAGCAG TTC NYU_E 65557650 65592691 InFrame 8334 ATGGCCTCGGAGAGTGGGAAGCTTTGGGGTGGCCGG TTTGTGGGTGCAGTGGACCCCATCATGGAGAAGTTCA ACGCGTCCATTGCCTACGACCGGCACCTTTGGGAGGT GGATGTTCAAGGCAGCAAAGCCTACAGCAGGGGCCTG GAGAAGGCAGGGCTCCTCACCAAGGCCGAGATGGAC CAGATACTCCATGGCCTAGACAAGGTGGCTGAGGAGT GGGCCCAGGGCACCTTCAAACTGAACTCCAATGATGA GGACATCCACACAGCCAATGAGCGCCGCCTGAAGGAG CTCATTGGTGCAACGGCAGGGAAGCTGCACACGGGAC GGAGCCGGAATGACCAGGTGGTCACAGACCTCAGGCT GTGGATGCGGCAGACCTGCTCCACGCTCTCGGGCCTCC TCTGGGAGCTCATTAGGACCATGGTGGATCGGGCAGA GGCGGAACGTGATGTTCTCTTCCCGGGGTACACCCATT TGCAGAGGGCCCAGCCCATCCGCTGGAGCCACTGGAT TCTGAGCCACGCCGTGGCACTGACCCGAGACTCTGAG CGGCTGCTGGAGGTGCGGAAGCGGATCAATGTCCTGC CCCTGGGGAGTGGGGCCATTGCAGGCAATCCCCTGGG TGTGGACCGAGAGCTGCTCCGAGCAGAACTCAACTTT GGGGCCATCACTCTCAACAGCATGGATGCCACTAGTG AGCGGGACTTTGTGGCCGAGTTCCTGTTCTGGGCTTCG CTGTGCATGACCCATCTCAGCAGGATGGCCGAGGACC TCATCCTCTACTGCACCAAGGAATTCAGCTTCGTGCAG CTCTCAGATGCCTACAGCACGGGAAGCAGCCTGATGC CCCAGAAGAAAAACCCCGACAGTTTGGAGCTGATCCG GAGCAAGGCTGGGCGTGTGTTTGGGCGGTGTGCCGG GCTCCTGATGACCCTCAAGGGACTTCCCAGCACCTACA ACAAAGACTTACAGGAGGACAAGGAAGCTGTGTTTGA AGTGTCAGACACTATGAGTGCCGTGCTCCAGGTGGCC ACTGGCGTCATCTCTACGCTGCAGATTCACCAAGAGAA CATGGGACAGGCTCTCAGCCCCGACATGCTGGCCACT GACCTTGCCTATTACCTGGTCCGCAAAGGGATGCCATT CCGCCAGGCCCACGAGGCCTCCGGGAAAGCTGTGTTC ATGGCCGAGACCAAGGGGGTCGCCCTCAACCAGCTGT CACTGCAGGAGCTGCAGACCATCAG|GAAGGATGCCA ATTCTGCGCTTCTCAGTAACTACGAGGTATTTCAGTTAC TAACTGATCTGAAAGAGCAGCGTAAAGAAAGTGGAAA GAATAAACACAGCTCTGGGCAACAGAACTTGAACACT ATCACCTATGAAACGTTAAAATACATATCAAAAACACC ATGCAGGCACCAGAGTCCTGAAATTGTCAGAGAATTTC TCACAGCATTGAAAAGCCACAAGTTGACCAAAGCTGA GAAGCTCCAGCTGCTGAACCACCGGCCTGTGACTGCT GTGGAGATCCAGCTGATGGTGGAAGAGAGTGAAGAG CGGCTCACGGAGGAGCAGATTGAAGCTCTTCTCCACA CCGTCACCAGCATTCTGCCTGCAGAGCCAGAGGCTGA GCAGAAGAAGAATACAAACAGCAATGTGGCAATGGAC GAAGAGGACCCAGCA G17816. 55268106 56079562 InFrame 8335 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-28- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 5215- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01A-01R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1850- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.4 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAG|GATGCT TTCATTGGATTTGGAGGAAATGTGATCAGGCAACAAG TCAAGGATAACGCCAAATGGTATATCACTGATTTTGTA GAGCTGCTGGGAGAACTGGAAGAA G17650. 55433922 55914330 InFrame 8336 ATGGGCGAGACCATGTCAAAGAGGCTGAAGCTCCACC TCGA-28- TGGGAGGGGAGGCAGAAATGGAGGAACGGGCGTTCG 2513- TCAACCCCTTCCCGGACTACGAGGCCGCCGCCGGGGC 01A-01R- GCTGCTCGCCTCCGGAGCGGCCGAAGAGACAGGCTGT 1850- GTTCGTCCCCCGGCGACCACGGATGAGCCCGGCCTCCC 01.2 TTTTCATCAGGACGGGAAG|CAAAAAGAAAATAATATT CGTTGTTTAACTACGATTGGACATTTTGGTTTGAATGT TTGCCCAATCAGTTGGTGAGCAGATCTATCCGACAAGG ATTCACTTTTAATATTCTCTGTGTGGGGGAGACTGGAA TTGGAAAATCGACACTGATAGACACATTGTTTAATACT AACTTGAAAGATAACAAATCCTCACATTTTTACTCAAAT GTTGGACTTCAAATTCAGACATATGAACTTCAGGAAAG CAATGTTCAGTTGAAATTGACTGTTGTGGAGACAGTAG GGTATGGTGATCAAATAGACAAAGAAGCCAGCTACCA ACCAATAGTTGACTACATAGATGCCCAATTTGAGGCCT ATCTTCAAGAAGAACTGAAGATTAAACGTTCCTTGTTT GAGTACCATGATTCTCGCGTCCACGTGTGTCTTTACTTC ATTTCACCTACAGGACATTCCCTGAAGTCTCTTGATCTA TTAACAATGAAGAACCTTGACAGTAAGGTGAATATTAT ACCACTGATTGCCAAAGCAGACACTATTTCTAAAAATG ATTTACAGACGTTTAAGAATAAGATAATGAGTGAATTG ATTAGCAATGGCATCCAGATATATCAGCTCCCAACAGA TGAAGAAACTGCTGCTCAAGCGAACTCCTCAGTTAGTG GGCTGTTACCCTTTGCTGTGGTAGGGAGTACAGATGA AGTGAAAGTTGGAAAAAGGATGGTCAGAGGCCGTCA CTACCCTTGGGGAGTTTTGCAAGTGGAAAATGAAAAT CACTGTGACTTCGTTAAGCTCCGAGATATGCTTCTTTGT ACCAATATGGAAAATCTAAAAGAAAAAACCCACACTCA GCACTATGAATGTTATAGGTACCAAAAACTGCAGAAA ATGGGCTTTACAGATGTGGGTCCAAACAACCAGCCAG TTAGTTTTCAAGAAATCTTTGAAGCCAAAAGACAAGAG TTCTATGATCAATGTCAGAGGGAAGAAGAAGAGTTGA AACAGAGATTTATGCAGCGAGTCAAGGAGAAAGAAGC AACATTTAAAGAAGCTGAAAAAGAGCTGCAGGACAAG TTCGAGCATCTTAAAATGATTCAACAGGAGGAGATAA GGAAGCTCGAGGAAGAGAAAAAACAACTGGAAGGAG AAATCATAGATTTTTATAAAATGAAAGCTGCCTCCGAA GCACTGCAGACTCAGCTGAGCACCGATACAAAGAAAG ACAAACATCGTAAGAAA BT308 33222419 33303169 InFrame 8337 ATGGCGGCTCCCTTGGTCCTGGTGCTGGTGGTGGCTG TGACAGTGCGGGCGGCCTTGTTCCGCTCCAGTCTGGCC GAGTTCATTTCCGAGCGGGTGGAGGTGGTGTCCCCAC TGAGCTCTTGGAAGAGAGTGGTTGAAGGCCTTTCACT GTTGGACTTGGGAGTATCTCCGTATTCTGGAGCAGTAT TTCATGAAACTCCATTAATAATATACCTCTTTCATTTCCT AATTGACTATGCTGAATTGGTGTTTATGATAACTGATG CACTCACTGCTATTGCCCTGTATTTTGCAATCCAGGACT TCAATAAAGTTGTGTTTAAAAAGCAGAAACTCCTCCTA GAACTGGACCAGTATGCCCCAGATGTGGCCGAACTCA TCCGGACCCCTATGGAAATGCGTTACATCCCTTTGAAA GTGGCCCTGTTCTATCTCTTAAATCCTTACACGATTTTG TCTTGTGTTGCCAAGTCTACCTGTGCCATCAACAACACC CTCATTGCTTTCTTCATTTTGACTACGATAAAAG|ACAT AACCAGTGCGGTGCAATCCAAGCGAAGAAAATCCAAG G17656. 55268106 55588823 InFrame 8338 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-28- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 2514- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01A-02R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1850- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.2 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAG|TGCACA GAAGCCAAAAAGCATTGCTGGTATTTCGAAGGACTCT ATCCAACCTATTATATATGCCGCTCCTACGAGGACTGC TGTGGCTCCAGGTGCTGTGTGCGGGCCCTCTCCATACA GAGGCTGTGGTACTTCTGGTTCCTTCTGATGATGGGCG TGCTTTTCTGCTGCGGAGCCGGCTTCTTCATCCGGAGG CGCATGTACCCCCCGCCGCTGATCGAGGAGCCAGCCTT CAATGTGTCCTACACCAGGCAGCCCCCAAATCCCGGCC CAGGAGCCCAGCAGCCGGGGCCGCCCTATTACACCGA CCCAGGAGGACCGGGGATGAACCCTGTCGGGAATTCC ATGGCAATGGCTTTCCAGGTCCCACCCAACTCACCCCA GGGGAGTGTGGCCTGCCCGCCCCCTCCAGCCTACTGC AACACGCCTCCGCCCCCGTACGAACAGGTAGTGAAGG CCAAG G17639. 33295425 34382867 InFrame 8339 ATGGCGGAGGCGCCTCCTGTCTCAGGTACTTTTAAATT TCGA-12- CAATACAGATGCTGCTGAATTCATTCCTCAGGAGAAAA 3652- AAAATTCTGGTCTAAATTGTGGGACTCAAAGGAGACT 01A-01R- AGACTCTAATAGGATTGGTAGAAGAAATTACAGTTCAC 1849- CACCTCCCTGTCACCTTTCCAGGCAGGTCCCTTATGATG 01.2 AAATCTCTGCTGTTCATCAGCATAGTTATCATCCGTCAG GAAGCAAACCTAAGAGTCAGCAGACGTCTTTCCAGTCC TCTCCTTGTAATAAATCGCCCAAGAGCCATGGCCTTCA GAATCAACCTTGGCAGAAATTGAGGAATGAGAAGCAC CATATCAGAGTCAAGAAAGCACAGAGTCTTGCTGAGC AGACCTCAGATACAGCTGGATTAGAGAGCTCGACCAG ATCAGAGAGTGGGACAGACCTCAGAGAGCATAGTCCT TCTGAGAGTGAGAAGGAAGTTGTGGGTGCAGATCCCA GGGGAGCAAAACCCAAAAAAGCAACACAGTTTGTATA CAGCTATGGTAGAGGACCAAAAGTCAAGGGGAAACTC AAATGTGAATGGAGTAACCGAACAACTCCAAAACCGG AGGATGCTGGACCCGAAAGTACCAAACCTGTGGGGGT TTTCCACCCTGACTCTTCAGAGGCATCCTCTAGAAAAG GAGTATTGGATGGGTATGGAGCCAGACGAAATGAGC AGAGAAGATACCCACAGAAAAGGCCTCCCTGGGAAGT GGAGGGGGCCAGGCCACGACCAGGCAGAAATCCACC AAAACAGGAGGGCCACCGACATACAAACGCAGGACAC AGAAACAACATGGGCCCCATTCCAAAGGATGACCTCA ATGAAAGACCAGCAAAATCTACCTGTGACAGTGAGAA CTTGGCAGTCATCAACAAGTCTTCCAGGAGGGTTGACC AAGAGAAATGCACTGTACGGAGGCAGGATCCTCAAGT AGTATCTCCTTTCTCCCGAGGCAAACAGAACCATGTGC TAAAGAATGTGGAAACGCACACAG|CAGACAAATGCA GCCCAAACTACCTGGGCAGTGACTGGTACAACACATG GAGGATGGAACCTTACAACAGCAGCTGCTGCAACAAG TATACCACCTACCTTCCTCGGCTGCCTAAGGAGGCCAG GATGGAGACAGCAGTTCGAGGAATGCCCTTGGAATGC CCTCCTAGGCCGGAGCGGCTCAATGCCTACGAGCGCG AAGTGATGGTGAACATGCTGAACTCACTGTCGCGGAA CCAGCAGCTGCCGCGGATCACGCCCCGATGCGGGTGC GTGGACCCGCTGCCCGGCCGCCTGCCCTTCCATGGTTA CGAAAGTGCTTGCTCGGGCCGCCACTACTGTCTGCGCG GGATGGACTACTACGCCAGCGGGGCGCCCTGCACCGA CCGCCGCCTGCGGCCTTGGTGCCGGGAGCAACCGACT ATGTGTACCTCCCTACGAGCACCGGCCCGGAATGCAGT GTGCTGTTACAACTCCCCCGCCGTCATACTACCCATATC CGAACCT G17796. 58090156 57960909 InFrame 8340 ATGGCGGCGGAAACGCTGCTGTCCAGTTTGTTAGGAC TCGA-41- TGCTGCTTCTGGGACTCCTGTTACCCGCAAGTCTGACC 5651- GGCGGTGTCGGGAGCCTGAACCTGGAGGAGCTGAGT 01A-01R- GAGATGCGTTATGGGATCGAGATCCTGCCGTTGCCTGT 1850- CATGGGAGGGCAGAGCCAATCTTCGGACGTGGTGATT 01.4 GTCTCCTCTAAGTACAAACAGCGCTATGAGTGTCGCCT GCCAGCTGGAGCTATTCACTTCCAGCGTGAAAGGGAG GAGGAAACACCTGCTTACCAAGGGCCTGGGATCCCTG AGTTGTTGAGCCCAATGAGAGATGCTCCCTGCTTGCTG AAGACAAAGGACTGGTGGACATATGAATTCTGTTATG GACGCCACATCCAGCAATACCACATGGAAGATTCAGA GATCAAAGGTGAAGTCCTCTATCTCGGCTACTACCAAT CAGCCTTCGACTGGGATGATGAAACAGCCAAGGCCTC CAAGCAGCATCGTCTTAAACGCTACCACAGCCAGACCT ATGGCAATGGGTCCAAGTGCGACCTTAATGGGAGGCC CCGGGAGGCCGAGGTTCGG|GGTTGTACTGAACGCTT TGTGTCCAGCCCGGAGGAGATTCTGGATGTGATTGAT GAAGGGAAATCAAATCGTCATGTGGCTGTCACCAACA TGAATGAACACAGCTCTCGGAGCCACAGCATCTTCCTC ATCAACATCAAGCAGGAGAACATGGAAACGGAGCAG AAGCTCAGTGGGAAGCTGTATCTGGTGGACCTGGCAG GGAGTGAGAAGGTCAGCAAGACTGGAGCAGAGGGAG CCGTGCTGGACGAGGCAAAGAATATCAACAAGTCACT GTCAGCTCTGGGCAATGTGATCTCCGCACTGGCTGAG GGCACTAAAAGCTATGTTCCATATCGTGACAGCAAAAT GACAAGGATTCTCCAGGACTCTCTCGGGGGAAACTGC CGGACGACTATGTTCATCTGTTGCTCACCATCCAGTTAT AATGATGCAGAGACCAAGTCCACCCTGATGTTTGGGC AGCGGGCAAAGACCATTAAGAACACTGCCTCAGTAAA TTTGGAGTTGACTGCTGAGCAGTGgaagaagaaatatgag asggagaaggagaagacaaaggcccagaaggagaCGATTGCGA AGCTGGAGGCTGAGCTGAGCCGGTGGCGCAATGGAG AGAATGTGCCTGAGACAGAGCGCCTGGCTGGGGAGG AGGCAGCCCTGGGAGCCGAGCTCTGTGAGGAGACCCC TGTGAATGACAACTCATCCATCGTGGTGCGCATCGCGC CCGAGGAGCGGCAGAAATACGAGGAGGAGATCCGCC GTCTCTATAAGCAGCTTGACGACAAGGATGATGAAAT CAACCAACAAAGCCAACTCATAGAGAAGCTCAAGCAG CAAATGCTGGACCAGGAAGAGCTGCTGGTGTCCACCC GAGGAGACAACGAGAAGGTCCAGCGGGAGCTGAGCC ACCTGCAATCAGAGAACGATGCCGCTAAGGATGAGGT GAAGGAAGTGCTGCAGGCCCTGGAGGAGCTGGCTGT GAACTATGACCAGAAGTCCCAGGAGGTGGAGGAGAA GAGCCAGCAGAACCAGCTTCTGGTGGATGAGCTGTCT CAGAAGGTGGCCACCATGCTGTCCCTGGAGTCTGAGT TGCAGCGGCTACAGGAGGTCAGTGGACACCAGCGAA AACGAATTGCTGAGGTGCTGAACGGGCTGATGAAGGA TCTGAGCGAGTTCAGTGTCATTGTGGGCAACGGGGAG ATTAAGCTGCCAGTGGAGATCAGTGGGGCCATCGAGG AGGAGTTCACTGTGGCCCGACTCTACATCAGCAAAATC AAATCAGAAGTCAAGTCTGTGGTCAAGCGGTGCCGGC AGCTGGAGAACCTCCAGGTGGAGTGTCACCGCAAGAT GGAAGTGACCGGGCGGGAGCTCTCATCCTGCCAGCTC CTCATCTCTCAGCATGAGGCCAAGATCCGCTCGCTTAC GGAATACATGCAGAGCGTGGAGCTAAAGAAGCGGCA CCTGGAAGAGTCCTATGACTCCTTGAGCGATGAGCTG GCCAAGCTCCAGGCCCAGGAAACTGTGCATGAAGTGG CCCTGAAGGACAAGGAGCCTGACACTCAGGATGCAGA TGAAGTGAAGAAGGCTCTGGAGCTGCAGATGGAGAG TCACCGGGAGGCCCATCACCGGCAGCTGGCCCGGCTC CGGGACGAGATCAACGAGAAGCAGAAGACCATTGAT GAGCTCAAAGACCTAAATCAGAAGCTCCAGTTAGAGC TAGAGAAGCTTCAGGCTGACTACGAGAAGCTGAAGAG CGAAGAACACGAGAAGAGCACCAAGCTGCAGGAGCT GACATTTCTGTACGAGCGACATGAGCAGTCCAAGCAG GACCTCAAGGGTCTGGAGGAGACAGTTGCCCGGGAAC TCCAGACCCTCCACAACCTTCGCAAGCTGTTCGTTCAA GACGTCACGACTCGAGTCAAGAAAAGTGCAGAAATGG AGCCCGAAGACAGTGGGGGGATTCACTCCCAAAAGCA GAAGATTTCCTTTCTTGAGAACAACCTGGAACAGCTTA CAAAGGTTCACAAACAGCTGGTACGTGACAATGCAGA TCTGCGTTGTGAGCTTCCTAAATTGGAAAAACGACTTA GGGCTACGGCTGAGAGAGTTAAGGCCCTGGAGGGTG CACTGAAGGAGGCCAAGGAGGGCGCCATGAAGGACA AGCGCCGGTACCAGCAGGAGGTGGACCGCATCAAGG AGGCCGTTCGCTACAAGAGCTCGGGCAAACGGGGCCA TTCTGCCCAGATTGCCAAACCCGTCCGGCCTGGCCACT ACCCAGCATCCTCACCCACCAACCCCTATGGCACCCGG AGCCCTGAGTGCATCAGTTACACCAACAGCCTCTTCCA GAACTACCAGAATCTCTACCTGCAGGCCACACCCAGCT CCACCTCAGATATGTACTTTGCAAACTCCTGTACCAGC AGTGGAGCCACATCTTCTGGCGGCCCCTTGGCTTCCTA CCAGAAGGCCAACATGGACAATGGAAATGCCACAGAT ATCAATGACAATAGGAGTGACCTGCCGTGTGGCTATG AGGCTGAGGACCAGGCCAAGCTTTTCCCTCTCCACCAA GAGACAGCAGCCAGC G17468. 61554352 90122482 InFrame 8341 ATGAAGCTTGCTGACAGCGTAATGGCAGGGAAAGCTT TCGA-19- CCGACGGCTCCATCAAATGGCAGCTCTGCTACGACATC 0957- TCGGCCAGAACTTGGTGGATGGATGAATTTCATCCTTT 02A-11R- CATCGAAGCACTTCTGCCCCACGTCCGAGCCTTTGCCT 2005- ACACATGGTTCAACCTGCAGGCCCGAAAACGAAAATA 01.2 CTTCAAAAAACATGAAAAGCGTATGTCAAAAGAAGAA GAGAGAGCCGTGAAGGATGAATTGCTAAGTGAAAAA CCAGAGGTCAAGCAGAAGTGGGCATCTCGACTTCTGG CAAAGTTGCGGAAAGATATCCGACCCGAATATCGAGA GGATTTTGTTCTTACAGTTACAGGGAAAAAACCTCCAT GTTGTGTTCTTTCCAACCCAGACCAGAAAGGCAAGATG CGAAGAATTGACTGCCTCCGCCAGGCAGATAAAGTCT GGAGGTTGGACCTTGTTATGGTGATTTTGTTTAAAGGT ATTCCGCTGGAAAGTACTGATGGCGAGCGCCTTGTAA AGTCCCCACAATGCTCTAATCCAGGGCTCTGTGTCCAA CCCCATCACATAGGGGTTTCTGTTAAGGAACTCGATTT ATATTTGGCATACTTTGTGCATGCAGCAG|TAATTAGT GAATGCCAAAGGCAGCAACTGGAGGCTGTGAGCTACT CCTCTCGATATGCTCTGGGCCTCTTTTATGAAGCTGGT ACGAAGATTGATGTCCCTTGGGCTGGGCAGTACATCA CCAGTAATCCCTGCATACGCTTCGTCTCCATTGATAATA AGAAGCGCAATATAGAGTCATCAGAAATTGGGCCTTC CCTCGTGATTCACACCACTGTCCCATTTGGAGTTACATA CTTGGAACACAGCATTGAGGATGTGCAAGAGTTAGTC TTCCAGCAGCTGGAAAACATTTTGCCGGGTTTGCCTCA GCCAATTGCTACCAAATGCCAAAAATGGAGACATTCAC AGGTTACAAATGCTGCTGCCAACTGTCCTGGCCAAATG ACTCTGCATCACAAACCTTTCCTTGCATGTGGAGGGGA TGGATTTACTCAGTCCAACTTTGATGGCTGCATCACTTC TGCCCTATGTGTTCTGGAAGCTTTAAAGAATTATATT G17790. 20304379 20987526 InFrame 8342 ATGATGTTAAGAGGAAACCTGAAGCAAGTGCGCATTG TCGA-06- AGAAAAACCCGGCCCGCCTTCGCGCCCTGGAGTCCGC 5856- GGTGGGCGAGAGCGAGCCGGCGGCCGCGGCAGCCAT 01A-01R- GGCGCTCGCTCTTGCCGGGGAGCCGGCACCGCCCGCG 1849- CCCGCGCCTCCAGAGGACCACCCGGACGAGGAGATGG 01.4 GGTTCACTATCGACATCAAGAGTTTCCTCAAGCCGGGC GAGAAGACGTACACGCAGCGCTGCCGCCTCTTCGTGG GAAATCTGCCCACCGACATCACGGAGGAGGACTTCAA GAGGCTCTTCGAACGCTATGGCGAGCCCAGCGAAGTC TTCATCAACCGGGACCGTGGCTTCGGCTTCATCCGCTT GGAATCCAGAACCCTGGCTGAAATTGCAAAAGCAGAG CTGGACGGCACCATTCTCAAGAGCAGACCTCTACGGAT TCGCTTCGCTACACATGGAGCAGCCTTGACTGTCAAGA ACCTTTCTCCAGTTGTTTCCAATGAGCTGCTAGAGCAA GCATTTTCTCAGTTTGGTCCAGTAGAGAAAGCTGTTGT GGTTGTGGATGATCGCGGTAGAGCTACAGGAAAAGGT TTTGTAGAGTTTGCAGCAAAACCTCCTGCACGAAAGGC TCTGGAAAGATGTGGTGATGGGGCATTCTTGCTAACA ACGACCCCTCGTCCAGTCATTGTGGAACCCATGGAGCA GTTTGATGATGAAGATGGCTTGCCAGAGAAGCTGATG CAGAAAACTCAACAATATCATAAGGAAAGAGAACAAC CACCACGTTTTGCTCAACCTGGGACATTTGAATTTGAG TATGCATCTCGATGGAAGGCTCTTGATGAAATGGAAA AGCAGCAGCGTGAGCAGGTTGATAGAAACATCAGAG AAGCCAAAGAGAAACTGGAGGCAGAAATGGAAGCAG CTAGGCATGAACACCAATTAATGCTAATGAGGCAAGA TCTAATGAGGCGTCAAGAAGAACTCAGACGCTTGGAA GAACTCAGAAACCAAGAGTTGCAAAAACGGAAGCAAA TACAACTAAGACATGAAGAGGAGCATCGGCGGCGTGA GGAAGAAATGATCCGACACAGAGAACAGGAGGAACT GAGGCGACAGCAAGAGGGCTTTAAGCCAAACTACATG GAAAAT|GAAGGAATCGTGTCTCCTAGTGACCTGGACC TTGTCATGTCAGAAGGGTTGGGCATGCGGTATGCATTC ATTGGACCCCTGGAAACCATGCATCTCAATGCAGAAG GTATGTTAAGCTACTGCGACAGATACAGCGAAGGCAT AAAACATGTCCTACAGACTTTTGGACCCATTCCAGAGT TTTCCAGGGCCACTGCTGAGAAGGTTAACCAGGACAT GTGCATGAAGGTCCCTGATGACCCGGAGCACTTAGCT GCCAGGAGGCAGTGGAGGGACGAGTGCCTCATGAGA CTCGCCAAGTTGAAGAGTCAAGTGCAGCCCCAG GBM- 7470322 7217040 InFrame 8343 ATGAAAGAGACTATACAAGGGACCGGGTCCTGGGGG CUMC3338_L1 CCTGAGCCTCCTGGACCCGGCATACCCCCAGCTTACTC AAGTCCCAGGCGGGAGCGTCTTCGTTGGCCCCCACCTC CCAAACCCCGACTCAAGTCAGGTGGAGGGTTTGGGCC AGATCCTGGGTCAGGGACCACAGTGCCAGCCAGACGC CTCCCTGTCCCCCGACCCTCTTTTGATGCCTCAGCAAGT gaagaggaggaagaagaggaggaggaggaggatgaagatgaagag gaggaAGTGGCAGCTTGGAGGCTGCCCCCAAGATGGA GTCAGCTGGGAACCTCCCAGCGGCCCCGCCCTTCCCGC CCCACTCATCGAAAAACCTGCTCACAGCGCCGCCGCCG AGCCATGAGAGCCTTCCGGATGCTGCTCTACTCAAAAA GCACCTCGCTGACATTCCACTGGAAGCTTTgggggcgcca ccggggccggcggcggggccTCGCACACCCCAAGAACCATCT TTCACCCCAGCAAGGGGGTGCGACGCCACAGGTGCCA TCCCCCTGTTGTCGTTTTGACTCCCCCCGGGGGCCACCT CCACCCCGGCTGGGTCTGCTAGGTGCTCTCATGGCTGA GGATGGGGTGAGAGGGTCTCCACCAGTGCCCTCTGGG CCCCCCATGGAGGAAGATGGACTCAGGTGGACTCCAA AGTCTCCTCTGGACCCTGACTCGGGCCTCCTTTCATGTA CTCTGCCCAACGGTTTTGGGGGACAATCTGGGCCAGA AGGGGAGCGCAGCTTGGCACCCCCTGATGCCAGCATC CTCATCAGCAATGTGTGCAGCATCGGGGACCATGTGG CCCAGGAGCTTTTTCAGGGCTCAGATTTGGGCATGGCA GAAGAGGCAGAGAGGCCTGGGGAGAAAGCCGGCCA GCACAGCCCCCTGCGAGAGGAGCATGTGACCTGCGTA CAGAGCATCTTGGACGAATTCCTTCAAACGTATGGCAG CCTCATACCCCTCAGCACTGATGAGGTAGTAGAGAAG CTGGAGGACATTTTCCAGCAGGAGTTTTCCACCCCTTC CAGGAAGGGCCTGGTGTTGCAGCTGATCCAGTCTTAC CAGCGGATGCCAGGCAATGCCATGGTGAGGGGCTTCC GAGTGGCTTATAAGCGGCACGTGCTGACCATGGATGA CTTGGGGACCTTGTATGGACAGAACTGGCTCAATGAC CAGGTGATGAACATGTATGGAGACCTGGTCATGGACA CAGTCCCTGAAAAGGTGCATTTCTTCAATAGTTTCTTCT ATGATAAACTCCGTACCAAGGGTTATGATGGGGTGAA AAGGTGGACCAAAAAC|ACCCGGCACTACGTGGGCTC AGCAGCTGCTTTTGCAGGGACACCAGAGCATGGACAA TTCCAAGGCAGTCCTGGTGGTGCCTATGGGACTGCTCA GCCCCCACCTCACTATGGGCCCACACAGCCAGCTTATA GTCCTAGTCAGCAGCTCAGAGCTCCTTCGGCATTCCCT GCAGTGCAGTACCTATCTCAGCCACAGCCACAGCCCTA TGCTGTGCATGGCCACTTTCAGCCCACTCAGACAGGTT TCCTCCAGCCTGGTGGTGCCCTGTCCTTGCAAAAGCAG ATGGAACATGCTAACCAGCAGACTGGCTTCTCCGACTC ATCCTCTCTGCGCCCCATGCACCCCCAGGCTCTGCATCC AGCCCCTGGACTCCTTGCTTCCCCCCAGCTCCCTGTGCA GATGCAGCCAGCAGGAAAGTCGGGCTTTGCAGCTACC AGCCAACCTGGCCCTCGGCTCCCCTTCATCCAACACAG CCAGAACCCGCGATTCTACCACAAG G17790. 117175595 69229609 InFrame 8344 ATGGTGAACCTGGCGGCCATGGTGTGGCGCCGGCTTC TCGA-06- TGCGGAAGAGGTGGGTGCTCGCCCTGGTCTTCGGGCT 5856- GTCGCTCGTCTACTTCCTCAGCAGCACCTTCAAGCAG| 01A-01R- GATCTTGATGCTGGTGTAAGTGAACATTCAGGTGATTG 1849- GTTGGATCAGGATTCAGTUCAGATCAGTTTAGTGTAG 01.4 AATTTGAAGTTGAATCTCTCGACTCAGAAGATTATAGC CTTAGTGAAGAAGGACAAGAACTCTCAGATGAAGATG ATGAGGTATATCAAGTTACTGTGTATCAGGCAGGGGA GAGTGATACAGATTCATTTGAAGAAGATCCTGAAATTT CCTTAGCTGACTATTGGAAATGCACTTCATGCAATGAA ATGAATCCCCCCCTTCCATCACATTGCAACAGATGTTG GGCCCTTCGTGAGAATTGGCTTCCTGAAGATAAAGGG AAAGATAAAGGGGAAATCTCTGAGAAAGCCAAACTGG AAAACTCAACACAAGCTGAAGAGGGCTTTGATGTTCCT GATTGTAAAAAAACTATAGTGAATGATTCCAGAGAGT CATGTGTTGAGGAAAATGATGATAAAATTACACAAGC TTCACAATCACAAGAAAGTGAAGACTATTCTCAGCCAT CAACTTCTAGTAGCATTATTTATAGCAGCCAAGAAGAT GTGAAAGAGTTTGAAAGGGAAGAAACCCAAGACAAA GAAGAGAGTGTGGAATCTAGTTTGCCCCTTAATGCCAT TGAACCTTGTGTGATTTGTCAAGGTCGACCTAAAAATG GTTGCATTGTCCATGGCAAAACAGGACATCTTATGGCC TGCTTTACATGTGCAAAGAAGCTAAAGAAAAGGAATA AGCCCTGCCCAGTATGTAGACAACCAATTCAAATGATT GTGCTAACTTATTTCCCC G17802. 51203855 55886916 InFrame 8345 ATGGACGCGCCGCGCGCCTCGGCGGCCAAGCCCCCGA TCGA-28- CCGGGAGGAAGATGAAGGCTCGTGCTCCCCCACCTCC 5208- TGGAAAGGCTGCCACTCTGCATGTGCACAGTGACCAG 01A-01R- AAGCCCCCCCACGATGGGGCCCTCGGGTCGCAGCAGA 1850- ACTTGGTTCGCATGAAGGAGGCGCTGAGGGCCAGCAC 01.4 CATGGACGTCACCGTGGTCCTGCCTAGTGGGCTGGAG AAGAGGAGCGTGCTCAATGGGAGCCATGCGATGATG GACCTACTGGTTGAACTTTGCCTTCAGAACCACCTGAA TCCATCCCACCATGCCCTTGAAATTCGGTCTTCAGAAAC CCAACAACCTTTGAGTTTTAAGCCAAATACTTTGATTG GGACCCTGAATGTGCATACTGTGTTTCTGAAAGAAAAA GTTCCTGAAGAGAAGGTTAAGCCTGGTCCCCCTAAGG TGCCTGAGAAATCTGTGCGTTTGGTCGTGAATTACCTG CGGACACAAAAAGCTGTTGTGCGTGTGAGCCCTGAGG TTCCTCTCCAGAATATTCTCCCAGTCATTTGTGCAAAGT GTGAGGTCAGCCCAGAGCACGTGGTTCTCCTCAGGGA CAACATTGCCGGAGAGGAGCTGGAGCTGTCCAAGTCC CTGAACGAGCTCGGGATAAAGGAGCTCTACGCGTGGG ACAACAGAAGAGAAACCTTTAGGAAATCATCACTTGG CAATGATGAGACAGATAAAGAGAAGAAAAAATTTCTG GGATTTTTCAAAGTTAATAAAAGAAGCAATAGTAAGG CTGAGCAGCTCGTGCTGTCGGGTGCAGACAGCGATGA GGACACCTCCAGGGCTGCCCCAGGAAGGGGTTTGAAC GGCTGTTTAACGACCCCCAACTCCCCATCCATGCACTC ACGTTCTCTTACGCTGGGTCCATCCCTCTCGCTGGGCA GCATCTCAGGGGTGTCCGTGAAGTCGGAGATGAAGAA GCGCCGAGCCCCTCCTCCTCCAGGTTCAGGGCCACCTG TGCAAGACAAGGCATCGGAAAAG|GGGCTGTTACCCT TTGCTGTGGTAGGGAGTACAGATGAAGTGAAAGTTGG AAAAAGGATGGTCAGAGGCCGTCACTACCCTTGGGGA GTTTTGCAAGTGGAAAATGAAAATCACTGTGACTTCGT TAAGCTCCGAGATATGCTTCTTTGTACCAATATGGAAA ATCTAAAAGAAAAAACCCACACTCAGCACTATGAATGT TATAGGTACCAAAAACTGCAGAAAATGGGCTTTACAG ATGTGGGTCCAAACAACCAGCCAGTTAGTTTTCAAGAA ATCTTTGAAGCCAAAAGACAAGAGTTCTATGATCAATG TCAGAGGGAAGAAGAAGAGTTGAAACAGAGATTTAT GCAGCGAGTCAAGGAGAAAGAAGCAACATTTAAAGA AGCTGAAAAAGAGCTGCAGGACAAGTTCGAGCATCTT AAAATGATTCAACAGGAGGAGATAAGGAAGCTCGAG GAAGAGAAAAAACAACTGGAAGGAGAAATCATAGATT TTTATAAAATGAAAGCTGCCTCCGAAGCACTGCAGACT CAGCTGAGCACCGATACAAAGAAAGACAAACATCGTA AGAAA G17210. 101176424 30536851 InFrame 8346 ATGAAGCTGGCCCTGCTCCTGCCCTGGGCGTGTTGCTG TCGA-12- CCTCTGCGGGTCGGCGCTGGCCACCGGCTTCCTCTATC 0616- CCTTCTCGGCCGCAGCTCTGCAGCAGCACGGCTACCCC 01A-01R- GAGCCCGGCGCCGGCTCCCCTGGCAGCGGCTACGCGA 1849- GCCGCCGGCACTGGTGCCATCACACAGTGACACGGAC 01.2 GGTGTCCTGCCAGGTGCAGAATGGCTCGGAGACGGTG GTCCAGCGCGTGTACCAGAGCTGCCGGTGGCCGGGGC CCTGCGCCAACCTCGTAAGTTACAGGACTCTGATCAGA CCCACCTACAGAGTGTCCTACCGCACGGTGACGGTGCT GGAGTGGAGATGCTGCCCTGGCTTCACCGGGAGCAAC TGTGATGAGGAATGCATGAACTGCACCCGGCTCAGTG ACATGAGTGAGCGACTGACCACACTGGAGGCCAAG|A TTATTTGCATGGGTGCAAAAGAAAATGGTTTGCCGCTG GAGTATCAAGAGAAGTTAAAAGCAATAGAACCAAATG ACTATACAGGAAAGGTCTCAGAAGAAATTGAAGACAT CATCAAAAAGGGGGAAACACAAACTCTT NYU_B 233613792 234862561 InFrame 8347 ATGGCAGCGGAAACGCAGACACTGAACTTTGGGCCTG AATGGCTCCGAGCTCTGTCCAGTGGTGGGAGTATTAC ATCCCCTCCTCTTTCTCCAGCATTGCCGAAGTATAAATT AGCAGATTATCGTTACGGCAGAGAAGAAATGTTAGCA CTTTTCCTTAAAGACAACAAGATACCTTCAGACCTTCTG GATAAAGAATTTCTGCCTATCCTCCAGGAGGAACCCCT TCCACCATTGGCTCTGGTACCCTTTACAGAAGAAGAAC AG|CTCAAAGAAATTCTCGAATGTTCTCACCTATTAACA GTTATTAAAATGGAAGAAGCTGGGGATGAAATTGTGA GCAATGCCATCTCCTACGCTCTATACAAAGCCTTCAGC ACCAGTGAGCAAGACAAGGATAACTGGAATGGGCAG CTGAAGCTTCTGCTGGAGTGGAACCAGCTGGACTTAG CCAATGATGAGATTTTCACCAATGACCGCCGATGGGA GTCTGCTGACCTTCAAGAAGTCATGTTTACGGCTCTCA TAAAGGACAGACCCAAGTTTGTCCGCCTCTTTCTGGAG AATGGCTTGAACCTACGGAAGTTTCTCACCCATGATGT CCTCACTGAACTCTTCTCCAACCACTTCAGCACGCTTGT GTACCGGAATCTGCAGATCGCCAAGAATTCCTATAATG ATGCCCTCCTCACGTTTGTCTGGAAACTGGTTGCGAAC TTCCGAAGAGGCTTCCGGAAGGAAGACAGAAATGGCC GGGACGAGATGGACATAGAACTCCACGACGTGTCTCC TATTACTCGGCACCCCCTGCAAGCTCTCTTCATCTGGGC CATTCTTCAGAATAAGAAGGAACTCTCCAAAGTCATTT GGGAGCAGACCAGGGGCTGCACTCTGGCAGCCCTGG GAGCCAGCAAGCTTCTGAAGACTCTGGCCAAAGTGAA GAACGACATCAATGCTGCTGGGGAGTCCGAGGAGCTG GCTAATGAGTACGAGACCCGGGCTGTTGAGCTGTTCA CTGAGTGTTACAGCAGCGATGAAGACTTGGCAGAACA GCTGCTGGTCTATTCCTGTGAAGCTTGGGGTGGAAGC AACTGTCTGGAGCTGGCGGTGGAGGCCACAGACCAGC ATTTCATCGCCCAGCCTGGGGTCCAGAATTTTCTTTCTA AGCAATGGTATGGAGAGATTTCCCGAGACACCAAGAA CTGGAAGATTATCCTGTGTCTGTTTATTATACCCTTGGT GGGCTGTGGCTTTGTATCATTTAGGAAGAAACCTGTCG ACAAGCACAAGAAGCTGCTTTGGTACTATGTGGCGTTC TTCACCTCCCCCTTCGTGGTCTTCTCCTGGAATGTGGTC TTCTACATCGCCTTCCTCCTGCTGTTTGCCTACGTGCTG CTCATGGATTTCCATTCGGTGCCACACCCCCCCGAGCT GGTCCTGTACTCGCTGGTCTTTGTCCTCTTCTGTGATGA AGTGAGACAGTGGTACGTAAATGGGGTGAATTATTTT ACTGACCTGTGGAATGTGATGGACACGCTGGGGCTTT TTTACTTCATAGCAGGAATTGTATTTCGGCTCCACTCTT CTAATAAAAGCTCTTTGTATTCTGGACGAGTCATTTTCT GTCTGGACTACATTATTTTCACTCTAAGATTGATCCACA TTTTTACTGTAAGCAGAAACTTAGGACCCAAGATTATA ATGCTGCAGAGGATGCTGATCGATGTGTTCTTCTTCCT GTTCCTCTTTGCGGTGTGGATGGTGGCCTTTGGCGTGG CCAGGCAAGGGATCCTTAGGCAGAATGAGCAGCGCTG GAGGTGGATATTCCGTTCGGTCATCTACGAGCCCTACC TGGCCATGTTCGGCCAGGTGCCCAGTGACGTGGATGG TACCACGTATGACTTTGCCCACTGCACCTTCACTGGGA ATGAGTCCAAGCCACTGTGTGTGGAGCTGGATGAGCA CAACCTGCCCCGGTTCCCCGAGTGGATCACCATCCCCC TGGTGTGCATCTACATGTTATCCACCAACATCCTGCTG GTCAACCTGCTGGTCGCCATGTTTGGCTACACGGTGGG CACCGTCCAGGAGAACAATGACCAGGTCTGGAAGTCC CAGAGGTACTTCCTGGTGCAGGAGTACTGCAGCCGCC TCAATATCCCCTTCCCCTTCATCGTCTTCGCTTACTTCTA CATGGTGGTGAAGAAGTGCTTCAAGTGTTGCTGCAAG GAGAAAAACATGGAGTCTTCTGTCTGCTGTTTCAAAAA TGAAGACAATGAGACTCTGGCATGGGAGGGTGTCATG AAGGAAAACTACCTTGTCAAGATCAACACAAAAGCCA ACGACACCTCAGAGGAAATGAGGCATCGATTTAGACA ACTGGATACAAAGCTTAATGATCTCAAGGGTCTTCTGA AAGAGATTGCTAATAAAATCAAA G17469. 55268106 55863785 InFrame 8348 ATGCGACCCTCCGGGACGGCCGGGGCAGCGCTCCTGG TCGA-06- CGCTGCTGGCTGCGCTCTGCCCGGCGAGTCGGGCTCT 2557- GGAGGAAAAGAAAGTTTGCCAAGGCACGAGTAACAA 01A-01R- GCTCACGCAGTTGGGCACTTTTGAAGATCATTTTCTCA 1849- GCCTCCAGAGGATGTTCAATAACTGTGAGGTGGTCCTT 01.2 GGGAATTTGGAAATTACCTATGTGCAGAGGAATTATG ATCTTTCCTTCTTAAAGACCATCCAGGAGGTGGCTGGT TATGTCCTCATTGCCCTCAACACAGTGGAGCGAATTCC TTTGGAAAACCTGCAGATCATCAGAGGAAATATGTACT ACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATG ATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAG AAATTTACAGGAAATCCTGCATGGCGCCGTGCGGTTCA GCAACAACCCTGCCCTGTGCAACGTGGAGAGCATCCA GTGGCGGGACATAGTCAGCAGTGACTTTCTCAGCAAC ATGTCGATGGACTTCCAGAACCACCTGGGCAGCTGCC AAAAGTGTGATCCAAGCTGTCCCAATGGGAGCTGCTG GGGTGCAGGAGAGGAGAACTGCCAGAAACTGACCAA AATCATCTGTGCCCAGCAGTGCTCCGGGCGCTGCCGTG GCAAGTCCCCCAGTGACTGCTGCCACAACCAGTGTGCT GCAGGCTGCACAGGCCCCCGGGAGAGCGACTGCCTG GTCTGCCGCAAATTCCGAGACGAAGCCACGTGCAAGG ACACCTGCCCCCCACTCATGCTCTACAACCCCACCACGT ACCAGATGGATGTGAACCCCGAGGGCAAATACAGCTT TGGTGCCACCTGCGTGAAGAAGTGTCCCCGTAATTATG TGGTGACAGATCACGGCTCGTGCGTCCGAGCCTGTGG GGCCGACAGCTATGAGATGGAGGAAGACGGCGTCCG CAAGTGTAAGAAGTGCGAAGGGCCTTGCCGCAAAGTG TGTAACGGAATAGGTATTGGTGAATTTAAAGACTCACT CTCCATAAATGCTACGAATATTAAACACTTCAAAAACT GCACCTCCATCAGTGGCGATCTCCACATCCTGCCGGTG GCATTTAGGGGTGACTCCTTCACACATACTCCTCCTCTG GATCCACAGGAACTGGATATTCTGAAAACCGTAAAGG AAATCACAGGGTTTTTGCTGATTCAGGCTTGGCCTGAA AACAGGACGGACCTCCATGCCTTTGAGAACCTAGAAA TCATACGCGGCAGGACCAAGCAACATGGTCAGTTTTCT CTTGCAGTCGTCAGCCTGAACATAACATCCTTGGGATT ACGCTCCCTCAAGGAGATAAGTGATGGAGATGTGATA ATTTCAGGAAACAAAAATTTGTGCTATGCAAATACAAT AAACTGGAAAAAACTGTTTGGGACCTCCGGTCAGAAA ACCAAAATTATAAGCAACAGAGGTGAAAACAGCTGCA AGGCCACAGGCCAGGTCTGCCATGCCTTGTGCTCCCCC GAGGGCTGCTGGGGCCCGGAGCCCAGGGACTGCGTC TCTTGCCGGAATGTCAGCCGAGGCAGGGAATGCGTGG ACAAGTGCAACCTTCTGGAGGGTGAGCCAAGGGAGTT TGTGGAGAACTCTGAGTGCATACAGTGCCACCCAGAG TGCCTGCCTCAGGCCATGAACATCACCTGCACAGGACG GGGACCAGACAACTGTATCCAGTGTGCCCACTACATTG ACGGCCCCCACTGCGTCAAGACCTGCCCGGCAGGAGT CATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCA GACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTG CACCTACGGATGCACTGGGCCAGGTCTTGAAGGCTGT CCAACGAATGGGCCTAAGATCCCGTCCATCGCCACTGG GATGGTGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCC CTGGGGATCGGCCTCTTCATGCGAAGGCGCCACATCG TTCGGAAGCGCACGCTGCGGAGGCTGCTGCAGGAGA GGGAGCTTGTGGAGCCTCTTACACCCAGTGGAGAAGC TCCCAACCAAGCTCTCTTGAGGATCTTGAAGGAAACTG AATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTT CGGCACGGTGTATAAGGGACTCTGGATCCCAGAAGGT GAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAA GAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCT CGATGAAGCCTACGTGATGGCCAGCGTGGACAACCCC CACGTGTGCCGCCTGCTGGGCATCTGCCTCACCTCCAC CGTGCAGCTCATCACGCAGCTCATGCCCTTCGGCTGCC TCCTGGACTATGTCCGGGAACACAAAGACAATATTGG CTCCCAGTACCTGCTCAACTGGTGTGTGCAGATCGCAA AGGGCATGAACTACTTGGAGGACCGTCGCTTGGTGCA CCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACA CCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCA AACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAG AAGGAGGCAAAGTGCCTATCAAGTGGATGGCATTGGA ATCAATTTTACACAGAATCTATACCCACCAGAGTGATG TCTGGAGCTACGGGGTGACTGTTTGGGAGTTGATGAC CTTTGGATCCAAGCCATATGACGGAATCCCTGCCAGCG AGATCTCCTCCATCCTGGAGAAAGGAGAACGCCTCCCT CAGCCACCCATATGTACCATCGATGTCTACATGATCAT GGTCAAGTGCTGGATGATAGACGCAGATAGTCGCCCA AAGTTCCGTGAGTTGATCATCGAATTCTCCAAAATGGC CCGAGACCCCCAGCGCTACCTTGTCATTCAG|CTGCAG GACAAGTTCGAGCATCTTAAAATGATTCAACAGGAGG AGATAAGGAAGCTCGAGGAAGAGAAAAAACAACTGG AAGGAGAAATCATAGATTTTTATAAAATGAAAGCTGCC TCCGAAGCACTGCAGACTCAGCTGAGCACCGATACAA AGAAAGACAAACATCGTAAGAAA G17480. 231945028 230377652 InFrame 8349 ATGATCACCTCGGCCGCTGGAATTATTTCTCTTCTGGAT TCGA-27- GAAGATGAACCACAGCTTAAGGAATTTGCACTACACA 1830- AATTGAATGCAGTTGTTAATGACTTCTGGGCAGAAATT 01A-01R- TCCGAGTCCGTAGACAAAATAGAGGTTTTATACGAAG 1850- ATGAAGGTTTCCGGAGTCGGCAGTTTGCAGCCTTAGT 01.2 GGCATCTAAAGTATTTTATCACCTGGGGGCTTTTGAGG AGTCTCTGAATTATGCTCTTGGAGCAGGGGACCTCTTC AATGTCAATGATAACTCTGAATATGTGGAAACTATTAT AGCAAAATGCATTGATCACTACACCAAACAATGTGTGG AAAATGCAGATTTGCCTGAAGGAGAAAAAAAACCAAT TGACCAGAGATTGGAAGGCATCGTAAATAAAATGTTC CAGCGATGTCTAGATGATCACAAGTATAAACAGGCTAT TGGCATTGCTCTGGAGACACGAAGACTGGACGTCTTT GAAAAGACCATACTGGAGTCGAATGATGTCCCAGGAA TGTTAGCTTATAGCCTTAAGCTCTGCATGTCTTTAATGC AGAATAAACAGTTTCGGAATAAAGTACTAAGAGTTCTA GTTAAAATCTACATGAACTTGGAGAAACCTGATTTCAT CAATGTTTGTCAGTGCTTAATTTTCTTAGATGATCCTCA GGCTGTGAGTGATATCTTAGAGAAACTGGTAAAGGAA GACAACCTCCTGATGGCATATCAGATTTGTTTTGATTTG TATGAAAGTGCTAGCCAGCAGTTTTTGTCATCTGTAAT CCAGAATCTTCGAACTGTTGGCACCCCTATTGCTTCTGT GCCTGGATCCACTAATACGGGTACTGTTCCGGGATCAG AGAAAGACAGTGACTCGATGGAAACAGAAGAAAAGA CAAGCAGTGCATTTGTAGGAAAGACACCAGAAGCCAG TCCAGAGCCTAAGGACCAGACTTTGAAAATGATTAAA ATTTTAAGTGGTGAAATGGCTATTGAGTTACATCTGCA GTTCTTAATACGAAACAATAATACAGACCTCATGATTC TAAAAAACACAAAGGATGCAGTACGGAATTCTGTATG TCATACTGCAACCGTTATAGCAAACTCTTTTATGCACTG TGGGACAACCAGTGACCAGTTTCTTAGAGATAATTTGG AATGGTTAGCCAGAGCCACTAACTGGGCAAAATTTACT GCTACAGCCAGTTTGGGTGTAATTCATAAGGGTCATGA AAAAGAAGCATTACAGTTAATGGCAACATACCTTCCCA AGGATACTTCTCCAGGATCAGCCTATCAGGAAGGTGG AGGTCTCTATGCACTAGGTCTTATTCATGCCAATCATG GTGGTGATATAATTGACTATCTGCTTAATCAGCTTAAG AACGCCAGCAATGATTGCAACTTTTTCCTGTACCTGTG AGGAGCAGTACGTGGGTACTTTCTGTGAAGAATACGA TGCTTGCCAGAGGAAACCTTGCCAAAACAACGCGAGC TGTATTGATGCAAATGAAAAGCAAGATGGGAGCAATT TCACCTGTGTTTGCCTTCCTGGTTATACTGGAGAGCTTT GCCAGTCCAAGATTGATTACTGCATCCTAGACCCATGC AGAAATGGAGCAACATGCATTTCCAGTCTCAGTGGATT CACCTGCCAGTGTCCAGAAGGATACTTCGGATCTGCTT GTGAAGAAAAGGTGGACCCCTGCGCCTCGTCTCCGTG CCAGAACAACGGCACCTGCTATGTGGACGGGGTACAC TTTACCTGCAACTGCAGCCCGGGCTTCACAGGGCCGAC CTGTGCCCAGCTTATTGACTTCTGTGCCCTCAGCCCCTG TGCTCATGGCACGTGCCGCAGCGTGGGCACCAGCTAC AAATGCCTCTGTGATCCAGGTTACCATGGCCTCTACTG TGAGGAGGAATATAATGAGTGCCTCTCCGCTCCATGCC TGAATGCAGCCACCTGCAGGGACCTCGTTAATGGCTAT GAGTGTGTGTGCCTGGCAGAATACAAAGGAACACACT GTGAATTGTACAAGGATCCCTGCGCTAACGTCAGCTGT CTGAACGGAGCCACCTGTGACAGCGACGGCCTGAATG GCACGTGCATCTGTGCACCCGGGTTTACAGGTGAAGA GTGCGACATTGACATAAATGAATGTGACAGTAACCCCT GCCACCATGGTGGGAGCTGCCTGGACCAGCCCAATGG TTATAACTGCCACTGCCCGCATGGTTGGGTGGGAGCA AACTGTGAGATCCACCTCCAATGGAAGTCCGGGCACA TGGCGGAGAGCCTCACCAACATGCCACGGCACTCCCTC TACATCATCATTGGAGCCCTCTGCGTGGCCTTCATCCTT ATGCTGATCATCCTGATCGTGGGGATTTGCCGCATCAG CCGCATTGAATACCAGGGTTCTTCCAGGCCAGCCTATG AGGAGTTCTACAACTGCCGCAGCATCGACAGCGAGTT CAGCAATGCCATTGCATCCATCCGGCATGCCAGGTTTG GAAAGAAATCCCGGCCTGCAATGTATGATGTGAGCCC CATCGCCTATGAAGATTACAGTCCTGATGACAAACCCT TGGTCACACTGATTAAAACTAAAGATTTG G17634. 36424288 37967938 InFrame 8350 ATGGCGGAGGGCGCCCAGCCGCATCAGCCGCCTCAGC TCGA-19- TcgggcccggcgccgccgcccggggcATGAAGCGGGAGTCGG 2625- AGCTGGAGCTGCCGGTGCCCGGAGCGGGAGGAGACG 01A-01R- GAGCCGATCCCGGCCTGAGCAAGCGGCCGCGCACTGA 1850- GGAGGCGGCGGCCGACGGTGGCGGCGGGATGCAG|G 01.2 GGGAACTTGAGGTTAAGAACATGGACATGAAGCCGG GGTCAACCCTGAAGATCACAGGCAGCATCGCCGATGG CACTGATGGCTTTGTAATTAATCTGGGCCAGGGGACA GACAAGCTGAACCTGCATTTCAACCCTCGCTTCAGCGA ATCCACCATTGTCTGCAACTCATTGGACGGCAGCAACT GGGGGCAAGAACAACGGGAAGATCACCTGTGCTTCAG CCCAGGGTCAGAGGTCAAGTTCACAGTGACCTTTGAG AGTGACAAATTCAAGGTGAAGCTGCCAGATGGGCACG AGCTGACTTTTCCCAACAGGCTGGGTCACAGCCACCTG AGCTACCTGAGCGTAAGGGGCGGGTTCAACATGTCCT CTTTCAAGTTAAAAGAA G17654. 66313803 86374956 InFrame 8351 ATGGACCGGCCGGGGTTCGTGGCAGCGCTGGTGGCT TCGA-41- GGTGGGGTAGCAGGTGTTTCTGTTGACTTGATATTATT 4097- TCCTCTGGATACCATTAAAACCAGGCTGCAGAGTCCCC 01A-01R- AAGGATTTAGTAAGGCTGGTGGTTTTCATGGAATATAT 1850- GCTGGCGTTCCTTCTGCTGCTATTGGATCCTTTCCTAAT 01.2 GCTGCTGCATTTTTTATCACCTATGAATATGTGAAGTG GTTTTTGCATGCTGATTCATCTTCATATTTGACACCTAT GAAACATATGTTGGCTGCCTCTGCTGGAGAAGTGGTT GCCTGCCTGATTCGAGTTCCATCTGAAGTGGTTAAGCA GAGGGCACAGGTATCTGCTTCTACAAGAACATTTCAGA TTTTCTCTAACATCTTATATGAAGAGGGTATCCAAGGG TTGTATCGAGGCTATAAAAGCACAGTTTTAAGAGAG|A TAGAAGAAGTCAGAGATGCCATGGAAAATGAAATGAG AACCCAGCTTCGCCGACAGGCAGCTGCCCACACTGATC ACTTGCGAGATGTCCTTAGGGTACAAGAACAGGAATT GAAGTCTGAATTTGAGCAGAACCTGTCTGAGAAACTCT CTGAACAAGAATTACAATTTCGTCGTCTCAGTCAAGAG CAAGTTGACAACTTTACTCTGGATATAAATACTGCCTAT GCCAGACTCAGAGGAATCGAACAGGCTGTTCAGAGCC ATGCAGTTGCTGAAGAGGAAGCCAGAAAAGCCCACCA ACTCTGGCTTTCAGTGGAGGCATTAAAGTACAGCATGA AGACCTCATCTGCAGAAACACCTACTATCCCGCTGGGT AGTGCAGTTGAGGCCATCAAAGCCAACTGTTCTGATAA TGAATTCACCCAAGCTTTAACCGCAGCTATCCCTCCAG AGTCCCTGACCCGTGGGGTGTACAGTGAAGAGACCCT TAGAGCCCGTTTCTATGCTGTTCAAAAACTGGCCCGAA GGGTAGCAATGATTGATGAAACCAGAAATAGCTTGTA CCAGTACTTCCTCTCCTACCTACAGTCCCTGCTCCTATTC CCACCTCAGCAACTGAAGCCGCCCCCAGAGCTCTGCCC TGAGGATATAAACACATTTAAATTACTGTCATATGCTTC CTATTGCATTGAGCATGGTGATCTGGAGCTAGCAGCA AAGTTTGTCAATCAGCTGAAGGGGGAATCCAGACGAG TGGCACAGGACTGGCTGAAGGAAGCCCGAATGACCCT AGAAACGAAACAGATAGTGGAAATCCTGACAGCATAT GCCAGCGCCGTAGGAATAGGAACCACTCAGGTGCAGC CAGAG G17485. 142166712 246093239 InFrame 8352 ATGGGAGTCCCCAAGTTTTACAGATGGATCTCAGAGC TCGA-14- GGTATCCCTGTCTCAGCGAAGTGGTGAAAGAGCATCA 1402- G|GTGATCTGCAACTCTTTCACCATCTGTAATGCGGAG 02A-01R- ATGCAGGAAGTTGGTGTTGGCCTATATCCCAGTATCTC 2005- TTTGCTCAATCACAGCTGTGACCCCAACTGTTCGATTGT 01.2 GTTCAATGGGCCCCACCTCTTACTGCGAGCAGTCCGAG ACATCGAGGTGGGAGAGGAGCTCACCATCTGCTACCT GGATATGCTGATGACCAGTGAGGAGCGCCGGAAGCA GCTGAGGGACCAGTACTGCTTTGAATGTGACTGTTTCC GTTGCCAAACCCAGGACAAGGATGCTGATATGCTAAC TGGTGATGAGCAAGTATGGAAGGAAGTTCAAGAATCC CTGAAAAAAATTGAAGAACTGAAGGCACACTGGAAGT GGGAGCAGGTTCTGGCCATGTGCCAGGCAATCATAAG CAGCAATTCTGAACGGCTTCCCGATATCAACATCTACC AGCTGAAGGTGCTCGACTGCGCCATGGATGCCTGCAT CAACCTCGGCCTGTTGGAGGAAGCCTTGTTCTATGGTA CTCGGACCATGGAGCCATACAGGATTTTTTTCCCAGGA AGCCATCCCGTCAGAGGGGTTCAAGTGATGAAAGTTG GCAAACTGCAGCTACATCAAGGCATGTTTCCCCAAGCA ATGAAGAATCTGAGACTGGCTTTTGATATTATGAGAGT GACACATGGCAGAGAACACAGCCTGATTGAAGATTTG ATTCTACTTTTAGAAGAATGCGACGCCAACATCAGAGC ATCC G17498. 119976637 332025 InFrame 8353 atggccgccgccggcgccCGGCTCAgccccggccccggctcggggc TCGA-02- tccgggggcggccgAGGCTCTGCTTCCACCCGGGgccgccgc 2483- cactgctgccgctgctgctgctgttcctgctcctgctgccgccgccgccgc 01A-01R- tgctgGCCGGCGCCACCGCCGCTGCCTCGCGGGAGCCC 1849- GACAGCCCGTGCCGGCTGAAGACCGTCACGGTGTCCA 01.2 CACTGCCCGCCCTGCGGGAGAGCGACATCggctggagcg gcgcccgcgccggggccggggctgggaccggggccggagccgCCGC CGCCGCCGCGTCCCCGGGCTCTCCTGGCTCTGCCGGCA CCGCCGCCGAGTCGCGCCTCCTGCTCTTTGTGCGTAAC GAGCTGCCGGGGCGCATCGCGGTGCAGGACGACCTG GACAACACCGAGCTGCCCTTCTTCACCCTGGAGATGTC TGGCACAGCAGCGGACATCTCGCTGGTGCACTGGAGA CAGCAGTGGCTGGAGAATGGCACCTTGTACTTCCACGT CTCCATGAGCAGCTCCGGGCAGCTGGCCCAAGCCACC GCCCCCACTCTCCAGGAGCCCTCGGAGATTGTTGAGG AGCAGATGCACATCCTCCACATTTCTGTGATGGGTGGC CTCATCGCGCTGCTGCTGCTGCTGCTGGTGTTCACCGT GGCGCTGTACGCCCAGCGACGTTGGCAGAAGCGTCGC CGCATCCCCCAGAAGAGCGCAAGCACAGAAGCCACTC ATGAGATCCACTACATCCCATCTGTGCTGCTGGGTCCC CAGGCGCGGGAGAGCTTCCGTTCATCCCGGCTGCAAA CCCACAATTCCGTCATTGGCGTGCCCATCCGGGAGACT CCCATCCTGGATGACTATGACTGTGAGGAGGATGAGG AGCCACCTAGGCGGGCCAACCATGTCTCCCGCGAGGA CGAGTTTGGCAGCCAGGTGACCCACACTCTGGACAGT CTGGGACATCCAGGGGAAGAGAAGGTGGACTTTGAG AAGAAAG|ACCCAAGCCTGCCCAATGTGCAGGTGACC AGGCTGACACTCCTGTCGGAACAGGCTCCGGGGCCCG TCGTCATGGATCTCACAGGGGACCTGGCTGTTCTGAAG GACCAGGTGTTTGTCCTGAAGGAAGGTGTTGATTACA GAGTGAAGATCTCCTTCAAGGTCCACAGGGAGATTGT CAGCGGCCTCAAGTGTCTGCACCACACCTACCGCCGG GGCCTGCGCGTGGACAAGACCGTCTACATGGTGGGCA GCTATGGCCCGAGCGCCCAGGAGTATGAGTTTGTGAC TCCGGTGGAGGAAGCGCCGAGGGGTGCGCTGGTGCG GGGCCCCTATCTGGTGGTGTCCCTCTTCACCGACGATG ACAGGACGCACCACCTGTCCTGGGAGTGGGGTCTCTG CATCTGCCAGGACTGGAAGGAC G17799. 61109367 47345631 InFrame 8354 ATGCTGCGATTACAGATGACTGATGGTCATATAAGTTG TCGA-06- CACAGCAGTAGAATTTAGTTATATGTCAAAAATAAGCC 1804- TGAACACACCACCTGGAACTAAAGTTAAGCTCTCAGGC 01A-01R- ATTGTTGACATAAAAAATGGATTCCTGCTCTTGAATGA 1849- CTCTAACACCACAGTTCTTGGTGGTGAAGTGGAACACC 01.4 TTATTGAGAAATGGGAGTTACAGAGAAGCTTATCAAA ACACAATAGAAGCAATATTGGAACTGAAGGTGGACCA CCGCCTTTTGTGCCTTTTGGACAGAAGTGTGTATCTCAT GTCCAAGTGGATAGCAGAGAACTTGATCGAAGAAAAA CATTGCAAGTTACAATGCCTGTCAAACCTACAAATGAT AATGATGAATTTGAAAAGCAAAGGACGGCTGCTATTG CTGAAGTTGCAAAGAGCAAGGAAACCAAGACATTTGG AGGAGGTGGTGGTGGTGCTAGAAGTAATCTCAATATG AATGCTGCTGGTAACCGAAATAGGGAAGTTTTACAGA AAGAAAAGTCAACCAAATCAGAGGGAAAACATGAAG GTGTCTATAGAGAACTGGTTGATGAGAAAGCTCTGAA GCACATAACGGAAATGGGCTTCAGTAAGGAAGCATCG AGGCAAGCTCTTATGGATAATGGCAACAACTTAGAAG CAGCACTGAACGTACTTCTTACAAGCAATAAACAGAAA CCTGTTATGGGTCCTCCTCTGAGAGGTAGAGGAAAAG GCAGGGGGCGAATAAGATCTGAAGATGAAGAGGACC TGGGAAATGCAAGGCCATCAGCACCAAGCACATTATTT GATTTCTTGGAATCTAAAATGGGAACTTTGAATGTGGA AGAACCTAAATCACAGCCACAGCAGCTTCATCAGGGA CAATACAGATCATCAAATACTGAGCAAAATGGAGTAA AAGATAATAATCATCTGAGACATCCTCCTCGAAATGAT ACCAGGCAGCCAAGAAATGAAAAACCGCCTCGTTTTC AAAGAGACTCCCAAAATTCAAAGTCAGTTTTAGAAGG CAGTGGATTACCTAGAAATAGAGGTTCTGAAAGACCA AGTACTTCTTCAGTATCTGAAGTATGGGCTGAAGACAG AATCAAATGTGATAGACCGTATTCTAGATATGACAGAA CTAAAGATACTTCATATCCTTTAGGTTCTCAGCATAGTG ATGGTGCTTTTAAAAAAAGAGATAACTCTATGCAAAGC AGATCAGGAAAAGGTCCCTCCTTTGCAGAGGCAAAAG AAAATCCACTTCCTCAAGGATCTGTAGATTATAATAAT CAAAAACGTGGAAAAAGAGAAAGCCAAACATCTATTC CTGATTA11111 ATGACAGGAAATCACAAACAATAAAT AATGAAGCTTTCAGTGGTATAAAAATTGAAAAACATTT TAATGTAAATACTGATTATCAGAATCCAGTTCGAAGTA ATAGTTTCATTGGTGTTCCAAATGGAGAAGTAGAAATG CCACTGAAAGGAAGACGAATAGGACCTATTAAGCCAG CAGGACCTGTCACAGCTGTACCCTGTGATGATAAAATA TTTTACAATAGTGGGCCCAAACGAAGATCTGGGCCAAT TAAGCCAGAAAAAATACTAGAATCATCTATTCCTATGG AGTATGCAAAAATGTGGAAACCTGGAGATGAATGTTT TGCACTTTATTGGGAAGACAACAAGTTTTACCGGGCAG AAGTTGAAGCCCTCCATTCTTCGGGTATGACAGCAGTT GTTAAATTCATTGACTACGGAAACTATGAAGAGGTGCT ACTGAGCAATATCAAGCCCATTCAAACAGAGGCATGG |GGTTATGATCATAGCTACTACTTCATTGCAACCTTTAT TACTGACCACATCAGACATCATGCTAAATACCTGAATG CA G17660. 61655656 69872567 InFrame 8355 ATGGCAGATCCAGGAATGATGAGTCTTTTTGGCGAGG TCGA-06- ATGGGAATATTTTCAGTGAAGGTCTTGAAGGCCTCGG 5414- AGAATGTGGTTACCCGGAAAATCCAGTAAATCCTATG 01A-01R- GGTCAGCAAATGCCAATAGACCAAGGCTTTGCCTCTTT 1849- ACAGCCATCCCTTCATCATCCTTCAACTAATCAAAATCA 01.2 AACAAAGCTGACACATTTTGATCACTATAATCAGTATG AACAACAAAAGATGCATCTGATGGATCAGCCGAACAG AATGATGAGCAACACCCCTGGGAACGGACTCGCGTCT CCGCACTCGCAGTATCACACCCCTCCCGTTCCTCAGGT GCCCCATGGTGGCAGTGGTGGCGGTCAGATGGGTGTC TACCCTGGCATGCAGAATGAGAGGCATGGGCAATCCT TTGTGGACAGCAGCTCCATGTGGGGCCCCAGGGCTGT TCAGGTACCAGACCAGATACGAGCCCCCTACCAGCAG CAGCAGCCACAGCCGCAGCCACCGCAGCCGGCTCCGT CGGGGCCCCCTGCACAGGGCCACCCTCAGCACATGCA GCAGATGGGCAGCTATATGGCACGTGGGGATTTTTCC ATGCAGCAGCATGGTCAGCCACAGCAGAGGATGAGCC AGTTTTCCCAAGGCCAAGAGGGCCTCAATCAGGGAAA TCCTTTTATTGCCACCTCAGGACCTGGCCACTTGTCCCA CGTGCCCCAGCAGAGTCCCAGCATGGCACCTTCCTTGC GTCACTCGGTGCAGCAGTTCCATCACCACCCCTCTACT GCTCTCCATGGAGAATCCGTTGCCCACAGTCCCAGATT CTCCCCGAATCCTCCCCAACAAGGGGCTGTTAGGCCGC AAACCCTTAACTTTAGTTCTCGGAGCCAGACAGTCCCC TCTCCTACTATAAACAACTCAGGGCAGTATTCTCGATAT CCTTACAGTAACCTAAATCAGGGATTAGTTAACAATAC AGGGATGAATCAAAATTTAGGCCTTACAAATAATACTC CAATGAATCAGTCCGTACCAAGATACCCCAATGCTGTA GGATTCCCATCAAACAGTGGTCAAGGACTAATGCACC AGCAGCCCATCCACCCCAGTGGCTCACTTAACCAAATG AACACACAAACTATGCATCCTTCACAGCCTCAGGGAAC TTATGCCTCTCCACCTCCCATGTCACCCATGAAAGCAAT GAGTAATCCAGCAGGCACTCCTCCTCCACAAGTCAGGC CGGGAAGTGCTGGGATACCAATGGAAGTTGGCAGTTA TCCAAATATGCCCCATCCTCAGCCATCTCACCAGCCCCC TGGTGCCATGGGAATCGGACAGAGGAATATGGGCCCC AGAAACATGCAGCAGTCTCGTCCATTTATAGGCATGTC CTCGGCACCAAGGGAATTGACTGGGCACATGAGGCCA AATGGTTGTCCTGGTGTTGGCCTTGGAGACCCACAAGC AATCCAGGAACGACTGATACCTGGCCAACAACATCCTG GTCAACAGCCATCTTTTCAGCAGTTGCCAACCTGTCCTC CACTGCAGCCTCACCCGGGCTTGCACCACCAGTCTTCA CCTCCACACCCTCATCACCAGCCTTGGGCACAGCTCCA CCCATCACCCCAGAACACCCCGCAGAAAGTGCCTGTGC ATCAG|TTTGACGGTGAGAACATGTATATGAGCATGAC AGAGCCGAGCCAGGACTATGTGCCAGCCAGCCAGTCC TACCCTGGTCCAAGCCTGGAAAGTGAAGACTTCAACAT TCCACCAATTACTCCTCCTTCCCTCCCAGACCACTCGCT GGTGCACCTGAATGAAGTTGAGTCTGGTTACCATTCTC TGTGTCACCCCATGAACCATAATGGCCTGCTACCATTTC ATCCACAAAACATGGACCTCCCTGAAATCACAGTCTCC AATATGCTGGGCCAGGATGGAACACTGCTTTCTAATTC CATTTCTGTGATGCCAGATATACGAAACCCAGAAGGA ACTCAGTACAGTTCCCATCCTCAGATGGCAGCCATGAG ACCAAGGGGCCAGCCTGCAGACATCAGGCAGCAGCCA GGAATGATGCCACATGGCCAGCTGACTACCATTAACCA GTCACAGCTAAGTGCTCAACTTGGTTTGAATATGGGAG GAAGCAATGTTCCCCACAACTCACCATCTCCACCTGGA AGCAAGTCTGCAACTCCTTCACCATCCAGTTCAGTGCA TGAAGATGAAGGCGATGATACCTCTAAGATCAATGGT GGAGAGAAGCGGCCTGCCTCTGATATGGGGAAAAAA CCAAAAACTCCCAAAAAGAAGAAGAAGAAGGATCCCA ATGAGCCCCAGAAGCCTGTGTCTGCCTATGCGTTATTC TTTCGTGATACTCAGGCCGCCATCAAGGGCCAAAATCC AAACGCTACCTTTGGCGAAGTCTCTAAAATTGTGGCTT CAATGTGGGACGGTTTAGGAGAAGAGCAAAAACAGG TCTATAAAAAGAAAACCGAGGCTGCGAAGAAGGAGTA CCTGAAGCAACTCGCAGCATACAGAGCCAGCCTTGTAT CCAAGAGCTACAGTGAACCTGTTGACGTGAAGACATC TCAACCTCCTCAGCTGATCAATTCGAAGCCGTCGGTGT TCCATGGGCCCAGCCAGGCCCACTCGGCCCTGTACCTA AGTTCCCACTATCACCAACAACCGGGAATGAATCCTCA CCTAACTGCCATGCATCCTAGTCTCCCCAGGAACATAG CCCCCAAGCCGAATAACCAAATGCCAGTGACTGTCTCT ATAGCAAACATGGCTGTGTCCCCTCCTCCTCCCCTCCAG ATCAGCCCGCCTCTTCACCAGCATCTCAACATGCAGCA GCACCAGCCGCTCACCATGCAGCAGCCCCTTGGGAAC CAGCTCCCCATGCAGGTCCAGTCTGCCTTACACTCACC CACCATGCAGCRAGGATTTACTCTTCAACCCGACTATC AGACTATTATCAATCCTACATCTACAGCTGCACAAGTT GTCACCCAGGCAATGGAGTATGTGCGTTCGGGGTGCA GAAATCCTCCCCCACAACCGGTGGACTGGAATAACGA CTACTGCAGTAGTGGGGGCATGCAGAGGGACAAAGC ACTGTACCTTACT GBM- 67688936 55238868 InFrame 8356 ATGGCGAGCGCCTCGTACCACATTTCCAATTTGCTGGA CUMC3296_L1 AAAAATGACATCCAGCGACAAGGACTTTAGGTTTATG GCTACAAATGATTTGATGACGGAACTGCAGAAAGATT CCATCAAGTTGGATGATGATAGTGAAAGGAAAGTAGT GAAAATGATTTTGAAGTTATTGGAAGATAAAAATGGA GAGGTACAGAATTTAGCTGTCAAATGTCTTGGTCCTTT AGTGAGTAAAGTGAAAGAATACCAAGTAGAGACAATT GTAGATACCCTCTGCACTAACATGCTTTCTGATAAAGA ACAACTTCGAGACATTTCAAGTATTGGTCTTAAAACAG TAATTGGAGAACTTCCTCCAGCTTCCAGTGGCTCTGCA TTAGCTGCTAATGTATGTAAAAAGATTACTGGACGTCT TACAAGTGCAATAGCAAAACAGGAAGATGTCTCTGTTC AGCTAGAAGCCTTGGATATTATGGCTGATATGTTGAGC AG|ATGCACTGGGCCAGGTCTTGAAGGCTGTCCAACG AATGGGCCTAAGATCCCGTCCATCGCCACTGGGATGG TGGGGGCCCTCCTCTTGCTGCTGGTGGTGGCCCTGGG GATCGGCCTCTTCATGCGAAGGCGCCACATCGTTCGGA AGCGCACGCTGCGGAGGCTGCTGCAGGAGAGGGAGC TTGTGGAGCCTCTTACACCCAGTGGAGAAGCTCCCAAC CAAGCTCTCTTGAGGATCTTGAAGGAAACTGAATTCAA AAAGATCAAAGTGCTGGGCTCCGGTGCGTTCGGCACG GTGTATAAGGGACTCTGGATCCCAGAAGGTGAGAAAG TTAAAATTCCCGTCGCTATCAAGGAATTAAGAGAAGCA ACATCTCCGAAAGCCAACAAGGAAATCCTCGATGAAG CCTACGTGATGGCCAGCGTGGACAACCCCCACGTGTG CCGCCTGCTGGGCATCTGCCTCACCTCCACCGTGCAGC TCATCACGCAGCTCATGCCCTTCGGCTGCCTCCTGGAC TATGTCCGGGAACACAAAGACAATATTGGCTCCCAGTA CCTGCTCAACTGGTGTGTGCAGATCGCAAAGGGCATG AACTACTTGGAGGACCGTCGCTTGGTGCACCGCGACCT GGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCAT GTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTGG GTGCGGAAGAGAAAGAATACCATGCAGAAGGAGGCA AAGTGCCTATCAAGTGGATGGCATTGGAATCAATTTTA CACAGAATCTATACCCACCAGAGTGATGTCTGGAGCTA CGGGGTGACTGTTTGGGAGTTGATGACCTTTGGATCC AAGCCATATGACGGAATCCCTGCCAGCGAGATCTCCTC CATCCTGGAGAAAGGAGAACGCCTCCCTCAGCCACCC ATATGTACCATCGATGTCTACATGATCATGGTCAAGTG CTGGATGATAGACGCAGATAGTCGCCCAAAGTTCCGT GAGTTGATCATCGAATTCTCCAAAATGGCCCGAGACCC CCAGCGCTACCTTGTCATTCAGGGGGATGAAAGAATG CATTTGCCAAGTCCTACAGACTCCAACTTCTACCGTGCC CTGATGGATGAAGAAGACATGGACGACGTGGTGGAT GCCGACGAGTACCTCATCCCACAGCAGGGCTTCTTCAG CAGCCCCTCCACGTCACGGACTCCCCTCCTGAGCTCTCT GAGTGCAACCAGCAACAATTCCACCGTGGCTTGCATTG ATAGAAATGGGCTGCAAAGCTGTCCCATCAAGGAAGA CAGCTTCTTGCAGCGATACAGCTCAGACCCCACAGGCG CCTTGACTGAGGACAGCATAGACGACACCTTCCTCCCA GTGCCTGaATACATAAACCAGTCCGTTCCCAAAAGGCC CGCTGGCTCTGTGCAGAATCCTGTCTATCACAATCAGC CTCTGAACCCCGCGCCCAGCAGAGACCCACACTACCAG GACCCCCACAGCACTGCAGTGGGCAACCCCGAGTATC TCAACACTGTCCAGCCCACCTGTGTCAACAGCACATTC GACAGCCCTGCCCACTGGGCCCAGAAAGGCAGCCACC AAATTAGCCTGGACAACCCTGACTACCAGCAGGACTTC TTTCCCAAGGAAGCCAAGCCAAATGGCATCTTTAAGG GCTCCACAGCTGAAAATGCAGAATACCTAAGGGTCGC GCCACAAAGCAGTGAATTTATTGGAGCA G17505. 216844 1282739 InFrame 8357 ATGAATAACCTAAATGATCCCCCAAATTGGAATATCCG TCGA-06- GCCTAATTCCAGGGCGGATGGTGGTGATGGAAGCAG 2564- GTGGAATTATGCCCTGTTGGTTCCAATGCTGGGATTGG 01A-01R- CTGCTTTTC|GGGTTGGCTGTGTTCCGGCCGCAGAGCA 1849- CCGTCTGCGTGAGGAGATCCTGGCCAAGTTCCTGCACT 01.2 GGCTGATGAGTGTGTACGTCGTCGAGCTGCTCAGGTC TTTCTTTTATGTCACGGAGACCACGTTTCAAAAGAACA GGCTCTTTTTCTACCGGAAGAGTGTCTGGAGCAAGTTG CAAAGCATTGGAATCAGACAGCACTTGAAGAGGGTGC AGCTGCGGGAGCTGTCGGAAGCAGAGGTCAGGCAGC ATCGGGAAGCCAGGCCCGCCCTGCTGACGTCCAGACT CCGCTTCATCCCCAAGCCTGACGGGCTGCGGCCGATTG TGAACATGGACTACGTCGTGGGAGCCAGAACGTTCCG CAGAGAAAAGAGGGCCGAGCGTCTCACCTCGAGGGT GAAGGCACTGTTCAGCGTGCTCAACTACGAGCGGGCG CGGCGCCCCGGCCTCCTGGGCGCCTCTGTGCTGGGCC TGGACGATATCCACAGGGCCTGGCGCACCTTCGTGCT GCGTGTGCGGGCCCAGGACCCGCCGCCTGAGCTGTAC TTTGTCAAGGTGGATGTGACGGGCGCGTACGACACCA TCCCCCAGGACAGGCTCACGGAGGTCATCGCCAGCAT CATCAAACCCCAGAACACGTACTGCGTGCGTCGGTATG CCGTGGTCCAGAAGGCCGCCCATGGGCACGTCCGCAA GGCCTTCAAGAGCCACGTCTCTACCTTGACAGACCTCC AGCCGTACATGCGACAGTTCGTGGCTCACCTGCAGGA GACCAGCCCGCTGAGGGATGCCGTCGTCATCGAGCAG AGCTCCTCCCTGAATGAGGCCAGCAGTGGCCTCTTCGA CGTCTTCCTACGCTTCATGTGCCACCACGCCGTGCGCA TCAGGGGCAAGTCCTACGTCCAGTGCCAGGGGATCCC GCAGGGCTCCATCCTCTCCACGCTGCTCTGCAGCCTGT GCTACGGCGACATGGAGAACAAGCTGTTTGCGGGGAT TCGGCGGGACGGGCTGCTCCTGCGTTTGGTGGATGAT TTCTTGTTGGTGACACCTCACCTCACCCACGCGAAAAC CTTCCTCAGGACCCTGGTCCGAGGTGTCCCTGAGTATG GCTGCGTGGTGAACTTGCGGAAGACAGTGGTGAACTT CCCTGTAGAAGACGAGGCCCTGGGTGGCACGGCTTTT GTTCAGATGCCGGCCCACGGCCTATTCCCCTGGTGCGG CCTGCTGCTGGATACCCGGACCCTGGAGGTGCAGAGC GACTACTCCAGCTATGCCCGGACCTCCATCAGAGCCAG TCTCACCTTCAACCGCGGCTTCAAGGCTGGGAGGAAC ATGCGTCGCAAACTCTTTGGGGTCTTGCGGCTGAAGTG TCACAGCCTGTTTCTGGATTTGCAGGTGAACAGCCTCC AGACGGTGTGCACCAACATCTACAAGATCCTCCTGCTG CAGGCGTACAGGTTTCACGCATGTGTGCTGCAGCTCCC ATTTCATCAGCAAGTTTGGAAGAACCCCACATTTTTCCT GCGCGTCATCTCTGACACGGCCTCCCTCTGCTACTCCAT CCTGAAAGCCAAGAACGCAGGGATGTCGCTGGGGGC CAAGGGCGCCGCCGGCCCTCTGCCCTCCGAGGCCGTG CAGTGGCTGTGCCACCAAGCATTCCTGCTCAAGCTGAC TCGACACCGTGTCACCTACGTGCCACTCCTGGGGTCAC TCAGGACAGCCCAGACGCAGCTGAGTCGGAAGCTCCC GGGGACGACGCTGACTGCCCTGGAGGCCGCAGCCAAC CCGGCACTGCCCTCAGACTTCAAGACCATCCTGGAC G17798. 11313895 6880241 InFrame 8358 ATGCTTGGAACCGGACCTGCCGCCGCCACCACCGCTGC TCGA-32- CACCACATCTAGCAATGTGAGCGTCCTGCAGCAGTTTG 5222- CCAGTGGCCTAAAGAGCCGGAATGAGGAAACCAGGG 01A-01R- CCAAAGCCGCCAAGGAGCTCCAGCACTATGTCACCAT 1850- GGAACTCCGAGAGATGAGTCAAGAGGAGTCTACTCGC 01.4 TTCTATGACCAACTGAACCATCACATTTTTGAATTGGTT TCCAGCTCAGATGCCAATGAGAGGAAAGGTGGCATCT TGGCCATAGCTAGCCTCATAGGAGTGGAAGGTGGGAA TGCCACCCGAATTGGCAGATTTGCCAACTATCTTCGGA ACCTCCTCCCCTCCAATGACCCAGTTGTCATGGAAATG GCATCCAAGGCCATTGGCCGTCTTGCCATGGCAGGGG ACACTTTTACCGCTGAGTACGTGGAATTTGAGGTGAAG CGAGCCCTGGAATGGCTGGGTGCTGACCGCAATGAGG GCCGGAGACATGCAGCTGTCCTGGTTCTCCGTGAGCT GGCCATCAGCGTCCCTACCTTCTTCTTCCAGCAAGTGC AACCCTTCTTTGACAACATTTTTGTGGCCGTGTGGGAC CCCAAACAGGCCATCCGTGAGGGAGCTGTAGCCGCCC TTCGTGCCTGTCTGATTCTCACAACCCAGCGTGAGCCG AAGGAGATGCAGAAGCCTCAGTGGTACAGGCACACAT TTGAAGAAGCAGAGAAGGGATTTGATGAGACCTTGGC CAAAGAGAAGGGCATGAATCGGGATGATCGGATCCAT GGAGCCTTGTTGATCCTTAACGAGCTGGTCCGAATCAG CAGCATGGAGGGAGAG|agcgtttcccaaagtgtattctgcgg aacTAGCACCTACTGTGTTCTCAACACCGTGCCACCTAT AGAAGATGATCATGGGAACAGCAATAGTAGTCATGTA AAAATCTTTTTACCGAAAAAGCTGCTTGAATGTCTGCC GAAATGTTCAAGTTTACCAAAAGAGAGGCACCGCTGG AACACTAATGAGGAAATTGCAGCTTATTTAATAACATT TGAGAAACACGAAGAATGGCTAACCACCTCCCCTAAG ACAAGACCACAGAATGGCTCAATGATACTCTACAACAG GAAGAAAGTGAAATACAGGAAAGATGGGTATTGCTG GAAAAAGAGGAAAGATGGGAAAACGACCAGAGAGGA CCACATGAAACTCAAGGTCCAGGGAGTGGAGTGCTTG TACGGCTGCTATGTCCATTCCTCCATCATCCCCACCTTC CACCGGAGGTGCTACTGGCTCCTTCAGAACCCCGACAT CGTCCTGGTGCACTACCTGAACGTGCCGGCCATCGAG GACTGCGGCAAGCCTTGCGGCCCCATCCTCTGCTCCAT CAACACCGACAAGAAGGAGTGGGCGAAATGGACGAA AGAAGAGCTCATCGGGCAGCTGAAACCCATGTTCCAT GGCATCAAGTGGACCTGCAGCAATGGGAACAGCAGCT CAGGCTTCTCGGTGGAACAGCTGGTGCAGCAGATCCT CGACAGCCACCAGACCAAGCCCCAGCCGCGGACCCAC AACTGCCTCTGCACCGGCAGCCTGGGAGCTGGCGGCA GCGTGCATCACAAGTGTAACAGCGCCAAACACCGCAT CATCTCGCCCAAGGTGGAGCCACGGACAGGGGGGTAC GGGAGCCACTCGGAGGTGCAGCACAATGACGTGTCG GAGGGCAAGCACGAGCACAGCCACAGCAAGGGCTCC AGCCGTGAGAAGAGGAACGGCAAGGTGGCCAAGCCC GTGCTCCTGCACCAGAGCAGCACCGAGGTCTCCTCCAC CAACCAGGTGGAAGTCCCCGACACCACCCAGAGCTCC CCTGTGTCCATCAGCAGCGGGCTCAACAGCGACCCGG ACATGGTGGACAGCCCGGTGGTCACAGGTGTGTCCGG TATGGCGGTGGCCTCTGTGATGGGGAGCTTGTCCCAG AGCGCCACGGTGTTCATGTCAGAGGTCACCAATGAGG CCGTGTACACCATGTCCCCCACCGCTGGCCCCAACCAC CACCTCCTCTCACCTGACGCCTCTCAGGGCCTCGTCCTG GCCGTGAGCTCTGATGGCCACAAGTTCGCCTTTCCCAC CACGGGCAGCTCGGAGAGCCTGTCCATGCTGCCCACC AACGTGTCCGAAGAGCTGGTCCTCTCCACCACCCTCGA CGGTGGCCGGAAGATTCCAGAAACCACCATGAACTTT GACCCCGACTGTTTCCTTAATAACCCAAAGCAGGGCCA GACGTACGGGGGTGGAGGCCTGAAAGCCGAGATGGT CAGCTCCAACATCCGGCACTCGCCACCCGGGGAGCGG AGCTTCAGCTTTACCACCGTCCTCACCAAGGAGATCAA GACCGAGGACACCTCCTTCGAGCAGCAGATGGCCAAA GAAGCGTACTCCTCCTCCGCGGCGGCTGTGGCAGCCA GCTCCCTCACCCTGACCGCCGGCTCCAGCCTCCTGCCG TCGGGCGGCGGCCTGAGTCCCAGCACCACCCTGGAGC AGATGGACTTCAGCGCCATCGACTCCAACAAGGACTA CACGTCCAGCTTCAGCCAGACGGGCCACAGCCCCCAC ATCCACCAGACCCCCTCCCCGAGCTTCTTCCTGCAGGA CGCCAGCAAACCCCTCCCCGTCGAGCAGAACACCCACA GCAGCCTGAGTGACTCTGGGGGCACCTTCGTGATGCC CACGGTGAAAACGGAGGCCTCGTCCCAAACCAGCTCC TGCAGCGGTCACGTGGAGACGCGGATCGAGTCCACTT CCTCCCTCCACCTCATGCAGTTCCAGGCCAACTTCCAG GCCATGACGGCAGAAGGGGAGGTCACCATGGAGACC TCGCAGGCGGCGGAAGGGAGCGAGGTCCTGCTCAAG TCTGGGGAGCTGCAGGCTTGCAGCTCTGAGCACTACCT GCAGCCGGAGACCAACGGGGTAATCCGAAGCGCCGG CGGCGTCCCCATCCTCCCGGGCAACGTGGTGCAGGGA CTCTACCCCGTGGCCCAGCCCAGCCTCGGCAACGCCTC CAACATGGAGCTCAGCCTGGACCACTTTGACATCTCCT TCAGCAACCAGTTCTCCGACCTGATCAACGACTTCATCT CCGTGGAGGGGGGCAGCAGCACCATCTATGGGCACCA GCTGGTGTCGGGGGACAGCACGGCGCTCTCACAGTCA GAGGACGGGGCGCGGGCCCCCTTCACCCAGGCAGAG ATGTGCCTCCCCTGCTGTAGCCCCCAGCAGGGTAGCCT GCAGCTGAGCAGCTCGGAGGGCGGGGCCAGCACCAT GGCCTACATGCACGTCGCCGAGGTGGTCTCGGCCGCC TCGGCCCAGGGCACCCTAGGCATGCTGCAGCAGAGCG GACGGGTGTTCATGGTGACCGACTACTCCCCAGAGTG GTCTTACCCAGAGGGAGGAGTGAAGGTCCTCATCACA GGCCCGTGGCAAGAAGCCAGCAATAACTACAGCTGCC TGTTTGACCAGATCTCAGTGCCTGCATCCCTGATTCAG CCTGGGGTGCTGCGCTGCTACTGCCCAGCCCATGACAC TGGTCTTGTGACCCTACAAGTTGCCTTCAACAACCAGA TCATCTCCAACTCGGTGGTGTTTGAGTACAAAGCCCGG GCTCTGCCCACGCTCCCTTCCTCCCAGCACGACTGGCT GTCGTTGGACGATAACCAGTTCAGGATGTCCATCCTGG AACGACTGGAGCAGATGGAGAGGAGGATGGCCGAGA TGACGGGGTCCCAGCAGCACAAACAGGCGAGCGGAG GCGGCAGCAGTGGAGGCGGCAGCGGGAGCGGGAAT GGAGGGAGCCAGGCACAGTGTGCTTCTGGGACTGGG GCCTTGGGGAGCTGCTTTGAGAGCCGTGTGGTCGTGG TATGCGAGAAGATGATGAGCCGAGCCTGCTGGGCGAA GTCCAAGCACTTGATCCACTCAAAGACTTTCCGCGGAA TGACCCTACTCCACCTGGCCGCTGCCCAGGGCTATGCC ACCCTAATCCAGACCCTCATCAAATGGCGTACAAAGCA CGCGGATAGCATTGACCTGGAACTGGAAGTTGACCCC TTGAATGTGGACCACTTCTCCTGTACTCCTCTGATGTG GGCGTGTGCCCTAGGGCACTTGGAAGCTGCCGTCGTG CTGTACAAGTGGGACCGTCGGGCCATCTCGATTCCCGA CTCTCTAGGAAGGCTGCCTTTGGGAATTGCCAGGTCAC GGGGTCATGTGAAATTAGCAGAGTGTCTGGAGCACCT GCAGAGAGATGAGCAGGCTCAGCTGGGACAGAACCC CAGAATCCACTGTCCTGCAAGCGAAGAGCCCAGCACA GAGAGCTGGATGGCCCAGTGGCACAGCGAAGCCATCA GCTCTCCAGAAATACCCAAGGGAGTCACTGTTATTGCA AGCACCAACCCAGAGCTGAGAAGACCTCGTTCTGAAC CCTCTAATTACTACAGCAGTGAGAGCCACAAAGATTAT CCGGCTCCCAAAAAGCATAAATTGAACCCTGAGTACTT CCAGACAAGGCAGGAGAAGCTGCTTCCCACTGCACTG AGTCTGGAAGAGCCAAATATCAGGAAGCAAAGCCCTA GTTCTAAGCAGTCTGTCCCCGAGACACTCAGCCCCAGT GAAGGAGTGAGGGACTTCAGCCGGGAACTCTCCCCTC CCACTCCAGAGACTGCAGCATTTCAAGCCTCTGGATCT CAGCCTGTAGGAAAGTGGAATTCCAAAGATCTTTACAT TGGTGTGTCTACAGTACAGGTGACTGGAAATCCGAAG GGGACCAGTGTAGGAAAGGAGGCAGCACCTTCACAG GTGCGTCCACGGGAACCAATGAGTGTCCTGATGATGG CTAACAGAGAGGTGGTGAATACAGAGCTGGGGTCCTA CCGTGATAGTGCAGAAAATGAAGAATGCGGCCAGCCC ATGGATGACATACAGGTGAACATGATGACCTTGGCAG AACACATTATTGAAGCCACACCTGACCGAATCAAGCAG GAGAATTTTGTGCCCATGGAGTCCTCAGGATTGGAAA GAACAGACCCTGCCACCATTAGCAGTACAATGAGCTG GCTGGCCAGTTATCTAGCGGATGCTGACTGCCTTCCCA GTGCTGCCCAGATCCGAAGTGCATATAACGAGCCTCTA ACCCCTTCTTCTAATACCAGCTTGAGCCCTGTTGGCTCT CCCGTCAGTGAAATCGCTTTCGAGAAACCTAACCTTCC CTCCGCCGCGGATTGGTCAGAATTCCTGAGTGCATCTA CCAGTGAGAAGGTAGAGAATGAGTTTGCTCAGCTCAC TCTGTCTGATCATGAACAGAGAGAACTCTATGAGGCTG CCAGGCTTGTCCAGACAGCTTTCCGGAAATACAAGGG CCGACCCTTGCGGGAACAGCAAGAAGTAGCTGCTGCT GTTATTCAGCGTTGTTACAGAAAATATAAACAGTACGC ACTTTATAAAAAGATGACACAGGCTGCCATCCTTATCC AGAGCAAATTCCGAAGTTACTATGAACAAAAAAAATTC CAGCAGAGCCGACGGGCTGCTGTGCTCATCCAAAAGT ACTACCGAAGTTATAAGAAATGTGGCAAAAGACGGCA GGCTCGCCGGACGGCTGTGATTGTACAACAGAAACTC AGGAGCAGTTTGCTAACCAAAAAGCAGGATCAAGCTG CTCGAAAAATAATGAGGTTTCTTCGCCGCTGTCGCCAC AGCCCCCTGGTGGACCATAGGCTGTACAAAAGGAGTG AAAGAATTGAAAAAGGCCAAGGAACT GBM- 24640521 18659539 InFrame 8359 ATGGCCCGGGGCTACGGGGCCACGGTCAGCCTAGTCC CUMC3297_L1 TGCTGGGTCTGGGGCTGGCGCTGGCTGTCATTGTGCT GGCTGTGGTCCTCTCTCGACACCAGGCCCCATGTGGCC CCCAGGCCTTTGCCCACGCTGCTGTTGCCGCCGACTCC AAGGTCTGCTCGGATATTGGACG|GCAGGAAACTGCA TATCTTCTGGTTTACATGAAGATGGAGTGC GBM- 61083748 104375025 InFrame 8360 ATGTTTGTGTATGTGCTCACTCCCGGAGAGCAATCAGG CUMC3342_L1 GAGACGGCTCCCCGGCCAGACTTGGCTGATGTTTTCTT GTTTCTGTTTCAGCCTTCAGGATAATTCCTTCAGCAGCA CCACTGTAACAGAGTGTGACGAAGATCCAGTCTCTCTA CATGAAGACCAGACTGATTGCTCCAGTCTCAGAGATG AAAACAATAAAGAGAACTACCCCGACGCAGGGGCTCT GGTAGAAGAGCACGCGCCGCCCTCTTGGGAGCCGCAG CAGCAGAATGTAGAGGCGACCGTGCTGGTGGACAGC GTATTGCGACCCAGCATGGGCAACTTCAAGTCCAGGA AGCCCAAGTCCATCTTCAAAGCGGAGAGCGGGAGGA GCCACGGAGAAAGTCAGGAGACAGAGCATGTGGTAT CCAGCCAGTCAGAGTGTCAGGTGAGAGCAGGAACACC AGCTCATGAGAGTCCACAAAACAATGCCTTCAAGTGCC AAGAAACAGTGCGACTTCAACCAAG|GAGCCGCAAAG ACAGCCTGGAAAGTGACAGCTCCACGGCCATCATTCCC CATGAGCTGATTCGCACGCGGCAGCTTGAGAGCGTAC ATCTGAAATTCAACCAGGAGTCCGGAGCCCTCATTCCT CTCTGCCTAAGGGGCAGGCTCCTGCATGGACGGCACT TTACATATAAAAGTATCACAGGTGACATGGCCATCACG TTTGTCTCCACGGGAGTGGAAGGCGCCTTTGCCACTGA GGAGCATCCTTACGCGGCTCATGGACCCTGGTTACAAA TTCTGTTGACCGAAGAGTTTGTAGAGAAAATGTTGGA GGATTTAGAAGATTTGACTTCTCCAGAGGAATTCAAAC TTCCCAAAGAGTACAGCTGGCCTGAAAAGAAGCTGAA GGTCTCCATCCTGCCTGACGTGGTGTTCGACAGTCCGC TACAC G17500. 39438743 41808143 InFrame 8361 ATGCACTCAGCCGGGACTCCCGGGTTATCCTCGCGCCG TCGA-27- GACAGGCAACTCCACCAGCTTTCAACCAGGACCGCCAC 1831- CGCCGCCCCGgctgctgctgctgctgctgctTCTCCTGTCACTG 01A-01R- GTAAGCCGCGTCCCGGCACAGCCCGCTGCCTTCGGCA 1850- GGGCGTTGCTGTCCCCTGGTCTCGCGGGGGCTGCAGG 01.2 GGTCCCTGCTGAGGAGGCCATAGTGCTGGCGAACCGC GGACTCCGGGTGCCTTTCGGCCGTGAAGTCTGGCTGG ATCCCCTGCATGACCTGGTGTTGCAGGTGCAGCCCGG GGACCGCTGCGCGGTTTCGGTACTAGACAACGACGCA CTGGCCCAGCGACCGGGCCGCCTGAGTCCCAAGCGCT TCCCGTGCGACTTTGGCCCTGGCGAGGTGCGCTACTCT CACCTGGGCGCGCGCAGCCCGTCTCGGGACCGCGTCC GGCTGCAGCTGCGCTATGACGCGCCCGGAGGGGCAGT AGTGCTACCACTGGTACTGGAGGTGGAGGTGGTCTTC ACCCAGCTGGAGGTTGTGACTCGGAACTTGCCTCTGGT CGTGGAAGAGCTGCTGGGGACCAGCAATGCCCTGGAC GCGCGGAGCCTGGAGTTCGCCTTCCAGCCCGAGACAG AGGAGTGCCGCGTGGGCATCCTGTCCGGCTTGGGCGC GCTGCCTCGCTATGGAGAACTCCTCCACTACCCGCAGG TCCCTGGAGGAGCCAGAGAGGGAGGCGCCCCGGAGA CTCTCCTGATGGACTGCAAAGCTTTCCAGGAACTAGGC GTGCGCTATCGCCACACAGCCGCCAGTCGCTCACCAAA CAGGGACTGGATACCCATGGTGGTGGAGCTGCGTTCA CGAGGGGCTCCTGTGGGCAGCCCTGCTTTGAAACGCG AGCACTTCCAGGTTCTGGTGAGGATCCGAGGAGGGGC CGAGAACACTGCACCCAAGCCCAGTTTCGTGGCCATG ATGATGATGGAGGTGGACCAGTTTGTACTGACGGCCC TGACCCCAGACATGCTGGCAGCCGAGGATGCTGAGTC TCCCTCTGACCTGTTGATCTTCAACCTTACTTCTCCATTC CAGCCTGGCCAGGGCTACTTGGTGAGCACCGATGATC GCAGCCTGCCCCTTTCCTCCTTCACTCAGAGGGATCTG CGGCTCCTGAAGATTGCCTACCAGCCCCCTTCTGAAGA CTCTGACCAGGAGCGCCTCTTTGAACTGGAATTGGAG GTAGTGGATCTAGAAGGAGCAGCTTCAGACCCTTTTGC CTTCATGGTAGTGGTGAAGCCCATGAACACAATGGCTC CGGTGGTCACCCGGAATACCGGTCTTATTCTCTATGAG GGTCAGTCTCGGCCCCTCACAGGCCCTGCAGGCAGTG GTCCGCAAAACTTGGTCATCAGCGATGAGGATGACCT AGAAGCAGTGCGGCTAGAGGTGGTGGCTGGGCTCCG GCATGGTCACCTTGTCATTCTGGGTGCTTCCAGTGGCA GCTCTGCTCCCAAGAGCTTTACAGTGGCTGAGCTGGCA GCCGGCCAGGTGGTCTACCAGCATGATGACAGAGACG GCTCGCTGAGCGACAACCTGGTGCTTCGCATGGTGGA TGGAGGAGGCAGGCACCAGGTACAGTTTCTGTTCCCC ATCACCTTAGTGCCTGTGGATGACCAGCCACCTGTTCT CAATGCCAACACGGGGCTGACACTGGCAGAGGGTGA AACAGTGCCCATCCTGCCCCTTTCCCTGAGTGCAACTG ACATGGATTCAGATGATTCTCTGCTGCTTTTTGTGCTG GAGTCACCCTTCTTAACTACGGGGCATCTGCTTCTCCG CCAAACTCACCCTCCCCATGAGAAGCAGGAACTTCTCA GAGGCCTTTGGAGGAAGGAGGGGGCATTTTATGAGC GAACAGTGACAGAGTGGCAGCAGCAGGACATAACAG AGGGCAGGCTGTTCTATAGACACTCTGGGCCCCATAGT CCTGGGCCAGTCACAGACCAGTTCACATTTAGAGTCCA GGATAACCATGACCCTCCTAATCAGTCCGGGCTACAGC GGTTTGTGATTCGTATCCATCCTGTGGATCGCCTCCCTC CGGAGCTGGGCAGTGGCTGTCCCCTTCGTATGGTGGT ACAGGAATCCCAGCTCACACCACTGAGGAAGAAGTGG CTGCGCTACACTGACCTGGACACAGATGACCGAGAAC TACGTTACACAGTGACTCAGTCCCCCACAGACACAGAC GAAAATCACCTGCCAGCCCCACTGGGTACCTTGGTCTT GACTGACAACCCCTCAGTCGTGGTGACCCATTTTACCC AAGCCCAGATCAACCATCATAAAATTGCTTACAGACCC CCGGGTCAAGAACTGGGCGTGGCTACTCGAGTGGCCC AGTTCCAGTTCCAGGTGGAAGACCGAGCTGGGAATGT GGCTCCAGGTACCTTTACCCTTTACTTGCATCCCGTGGA CAACCAGCCACCTGAGATCCTCAACACCGGCTTCACTA TTCAGGAGAAGGGTCACCACATCCTGAGTGAGACAGA GTTGCACGTGAATGATGTAGACACTGATGTTGCCCATA TCTCTTTCACTCTCACTCAGGCACCCAAACATGGCCACA TGAGAGTGTCTGGACAGATCCTGCATGTAGGGGGTCT CTTCCACTTGGAGGACATAAAACAGGGCCGAGTTTCCT ATGCCCATAATGGGGACAAGTCCCTGACTGATAGCTG CTCCTTGGAAGTCAGTGACAGACATCATGTGGTGCCCA TCACTCTCAGAGTAAATGTCCGGCCAGTGGATGATGA AGTGCCCATACTGAGCCATCCTACTGGCACTCTGGAGT CCTATCTAGATGTCTTAGAAAATGGGGCTACTGAAATC ACTGCCAATGTTATTAAGGGGACCAATGAGGAAACTG ATGACTTGATGTTGACTTTCCTCTTGGAAGATCCACCTT TGTATGGGGAAATCTTGGTCAATGGCATTCCAGCAGA GCAGTTTACTCAAAGGGACATCTTGGAGGGCTCTGTTG TATATACCCACACCAGTGGTGAGATAGGCCTATTGCCT AAAGCGGATTCTTTTAACCTGAGTCTGTCAGATATGTC TCAAGAATGGAGAATTGGTGGCAATACTATCCAAGGA GTTACTATATGGGTGACCATCCTGCCTGTTGATAGCCA GGCCCCAGAAATCTTTGTAGGTGAACAGTTGATAGTA ATGGAAGGTGATAAAAGTGTTATAACATCAGTGCATA TAAGTGCTGAAGATGTCGACTCCCTGAATGATGACATC TTGTGCACTATAGTTATTCAGCCTACTTCAGGTTATGTT GAAAACATTTCTCCAGCACCAGGCTCTGAGAAATCAAG AGCAGGGATTGCCATAAGTGCTTTCAACTTGAAAGATC TCAGGCAGGGCCACATAAACTATGTCCAGAGTGTCCAT AAAGGGGTGGAACCTGTGGAGGACCGATTTGTATTTC GTTGTTCTGATGGCATTAACTTTTCAGAGAGACAGTTC TTCCCCATTGTAATCATTCCCACCAATGATGAACAGCCA GAGATGTTTATGAGAGAATTTATGGTGATGGAAGGCA TGAGTCTGGTAATTGATACACCCATTCTCAATGCTGCT GATGCTGATGTTCCCCTGGATGATTTAACTTTCACTATT ACCCAATTCCCCACTCATGGTCACATCATGAATCAGCT GATAAATGGCACGGTTTTGGTCGAAAGCTTCACCTTGG ATCAGATCATAGAGAGTTCCAGCATTATTTATGAGCAT GATGACTCCGAGACCCAGGAAGACAGTTTTGTGATTA AACTAACAGATGGGAAGCACTCTGTGGAAAAGACGGT CCTCATTATAGTTATCCCTGTTGATGATGAGACGCCCA GAATGACTATCAATAATGGACTAGAAATAGAAATTGG GGATACCAAGATTATCAACAACAAAATATTAATGGCAA CAGATTTAGATTCAGAAGACAAATCTTTGGTTTATATT ATTCGTTATGGGCCAGGACATGGCTTATTACAGAGAC GAAAACCTACTGGTGCCTTTGAAAATATCACACTGGGC ATGAATTTTACCCAGGATGAAGTAGACAGAAACTTAAT TCAGTATGTCCATTTGGGGCAAGAGGGCATTCGGGAC CTAATTAAATTTGATGTGACTGATGGAATAAATCCCCT CATAGATCGTTACTTTTATGTGTCCATCGGGAGCATTG ACATTGTCTTCCCTGATGTGATAAGTAAGGGAGTGTCC TTGAAAGAAGGTGGCAAAGTCACTCTTACAACAGACC TACTAAGCACTAGTGACTTGAACAGTCCTGATGAAAAC TTGGTTTTTACCATCACCAGGGCTCCCATGCGAGGTCA CCTGGAATGCACGGATCAGCCTGGTGTGTCCATCACGT CTTTCACTCAGCTGCAACTGGCTGGAAACAAAATCTAC TACATCCACACAGCTGATGATGAAGTGAAAATGGACA GTTTTGAGTTTCAAGTCACCGATGGACGTAACCCTGTC TTTCGGACATTCCGTATCTCCATTAGCGATGTGGACAA TAAAAAGCCAGTGGTCACCATCCACAAGCTGGTTGTCA GTGAAAGTGAAAACAAGCTGATTACTCCTTTTGAGCTC ACTGTCGAAGACAGAGATACTCCTGACAAGCTCCTGA AATTCACTATCACCCAGGTGCCTATTCATGGCCATCTCC TATTCAACAATACCAGACCTGTCATGGTTTTTACCAAGC AAGACTTGAATGAAAACTTAATCAGCTACAAACATGAT GGCACTGAGTCAAGTGAAGATAGCTTCTCCTTCACAGT GACTGATGGCACCCATACAGACTTCTATGTTTTTCCTGA TACGGTGTTTGAAACAAGGAGACCCCAAGTGATGAAG ATCCAGGTCTTGGCTGTTGACAACAGTGTCCCCCAAAT CGCAGTGAATAAGGGGGCCTCTACACTTCGCACTCTAG CCACTGGCCACTTGGGGTTCATGATCACAAGCAAAATA TTGAAAGTGGAGGACAGAGACAGCTTACACATTTCTCT TAGATTTATCGTGACAGAGGCCCCTCAACATGGATATC TTCTCAACCTGGACAAAGGCAACCACAGCATCACTCAG TTCACACAAGCTGACATTGATGACATGAAAATATGCTA TGTCTTAAGAGAAGGGGCTAATGCCACAAGTGATATG TTCTATTTTGCAGTTGAAGATGGTGGTGGAAACAAGTT AACGTACCAGAATTTTCGTCTGAATTGGGCATGGATCT CCTTTGAAAAGGAATATTACCTGGTCAATGAGGACTCC AAATTTCTAGATGTTGTTCTTAAACGTAGAGGTTACTT GGGAGAAACTTCTTTTATAAGTATTGGCACAAGAGAC AGAACTGCAGAAAAAGACAAAGACTTCAAGGGCAAA GCACAGAAACAAGTGCAGTTCAACCCAGGCCAGACCA GGGCCACATGGCGAGTGCGGATCCTGAGTGATGGGG AGCATGAGCAGTCTGAAACCTTTCAGGTGGTACTCTCA GAGCCCGTGCTGGCTGCCTTGGAATTCCCCACAGTCGC CACTGTTGAGATCGTTGATCCAGGAGATGAGCCAACT GTGTTTATTCCCCAGTCCAAATACTCCGTTGAAGAAGA TGTTGGTGAGCTGTTCATTCCCATCAGGAGGAGCGGA GATGTGAGCCAGGAGTTGATGGTGGTCTGTTATACCC AACAAGGAACAGCAACTGGAACTGTGCCGACTTCCGT GTTGTCTTACTCTGATTACATATCCAGGCCTGAGGACC ACACCAGTGTTGTCCGCTTTGACAAAGATGAACGGGA GAAACTGTGTCGGATAGTCATAATTGATGACTCTTTGT ACGAGGAGGAGGAAACCTTCCATGTCCTTCTGAGCAT GCCCATGGGGGGAAGAATCGGATCAGAGTTCCCAGG GGCTCAAGTTACAATCGTTCCTGACAAAGATGATGAAC CCATCTTTTACTTCGGTGATGTGGAATACTCTGTGGAT GAGAGTGCTGGCTATGTGGAAGTGCAGGTGTGGAGA ACGGGCACTGACCTGTCCAAGTCTTCTAGTGTCACAGT GAGGTCTCGGAAAACAGATCCTCCCTCTGCAGATGCTG GAACAGACTATGTGGGCATCAGCCGTAATTTAGATTTT GCACCTGGAGTCAACATGCAGCCTGTTCGTGTTGTCAT TCTGGATGACCTTGGACAACCAGCGCTGGAGGGAATT GAGAAATTTGAACTGGTGCTTCGCATGCCTATGAACGC AGCCCTTGGCGAGCCCAGCAAAGCCACAGTGTCCATA AATGACTCTGTCTCCGATTTGCCTAAGATGCAATTCAA AGAACGAATATATACTGGCAGCGAAAGTGATGGGCAG ATAGTTACAATGATCCATAGGACTGGGGATGTCCAGT ACAGATCTTCAGTGAGATGCTACACCCGGCAGGGGTC TGCACAGGTGATGATGGACTTTGAAGAACGCCCAAAC ACTGATACCTCCATCATCACATTCCTCCCTGGTGAGACA GAAAAGCCCTGCATTCTTGAGCTGATGGACGATGTGCT CTATGAGGAGGTAGAGGAGCTCCGCCTGGTACTCGGC ACTCCACAAAGCAACTCTCCCTTTGGGGCTGCAGTTGG TGAACAAAATGAAACTCTCATAAGGATCCGAGATGAT GCTGATAAGACTGTTATTAAATTTGGAGAAACCAAATT TAGTGTCACTGAACCCAAAGAACCTGGAGAGTCGGTG GTTATAAGAATTCCAGTGATTCGCCAAGGAGACACTTC AAAGGTTTCCATTGTGAGAGTCCACACCAAGGATGGC TCGGCCACCTCTGGAGAAGACTACCACCCTGTGTCAGA AGAAATTGAGTTTAAGGAAGGGGAAACCCAGCACGTG GTTGAAATCGAAGTTACCTTTGACGGGGTGAGAGAGA TGAGAGAGGCCTTCACTGTTCACCTAAAACCTGATGAA AATATGATAGCAGAGATGCAGTTGACGAAAGCCATTG TGTACATAGAAGAAATGAGCAGCATGGCAGATGTCAC TTTTCCTTCTGTCCCTCAAATTGTATCCCTGTTGATGTAT GACGACACTTCCAAAGCTAAGGAGAGTGCTGAACCCA TGTCTGGCTATCCTGTCATCTGTATCACAGCTTGCAACC CCAAATATTCAGACTACGATAAAACAGGCTCTATCTGT GCAAGTGAGAACATCAATGACACTTTGACGCGGTACC GGTGGCTGATTAGTGCACCTGCGGGCCCTGACGGTGT GACCAGCCCTATGAGAGAAGTGGACTTCGACACCTTTT TTACGTCATCCAAGATGGTCACACTGGACTCCATATAC TTTCAGCCTGGCTCCCGGGTACAGTGCGCAGCTCGTGC TGTGAACACCAATGGGGATGAAGGCCTGGAGCTCATG AGCCCTATTGTAACCATCAGCAGAGAAGAAGGTCTTTG TCAGCCCCGTGTACCTGGGGTTGTTGGAGCAGAGCCG TTCTCAGCTAAATTGCGCTACACAGGCCCTGAGGATGC AGACTACACAAACCTTATCAAGCTCACTGTCACAATGC CACACATAGATGGCATGCTCCCCGTGATCTCCACTAGA GAGCTTTCCAACTTTGAGCTCACCCTCAGCCCTGATGG CACAAGAGTTGGAAACCACAAGTGCTCCAACCTCCTG GATTATACTGAAGTGAAGACTCATTATGGTTTCTTGAC TGATGCTACCAAAAATCCAGAAATAATTGGAGAGACA TATCCTTACCAGTACAGCTTGTCCATCAGAGGTTCCACT ACCTTGCGCTTCTACCGGAACCTGAACCTAGAGGCCTG TTTATGGGAGTTCGTTAGCTACTATGACATGTCAGAAC TCCTTGCTGACTGTGGTGGCACCATTGGAACAGATGG ACAGTGTGGATGTGAAATTGGACCCCAAGGATTTGCG AATAGATACATTTCGAGCCAAAGGAGCAGGAGGGCA GCATGTTAATAAAACTGATAGTGCCGTCAGACTTGTCC ACATCCCCACAGGGCTAGTAGTAGAATGCCAACAAGA AAGATCACAGATAAAAAATAAAGAAATAGCCTTTCGT GTGTTGAGAGCTAGACTCTACCAGCAGATTATTGAGA AAGACAAGCGTCAGCAACAAAGTGCTAGAAAACTGCA GGTGGGAACAAGAGCCCAGTCAGAGCGAATTCGGAC ATATAATTTCACCCAGGATAGAGTCAGTGACCACAGG ATAGCATATGAAGTTCGTGATATTAAGGCTCAGTCTCA TTCCACGGGTGGTAGTCGTGACCCTGCACATTCCACAT TCCTATCCTTGGATTCTGTGAGATCACCTGGTATTCTCA TTATGACTTCTTCTGTTAGGAATTTTTATGTGGTGGGA AGGGCCTGGATCAGC G17212. 3410422 47221257 InFrame 8362 ATGGCCATAGAccggcggcgcgaggcggcgggcggcgggcctgg TCGA-06- gcggcagccggccccggccgaggagaacggctccctgccgcccgggg 0129- acgcggcggcctcggcgcccctcgggggacgcgcgggccccggcggc 01A-01R- ggcgcggAGATCCAGCCGCTGCCCCCACTGCATCCTGGA 1849- GGCGGCCCGCACCCGAGCTGCTGCTCCGCGGCTGCGG 01.2 CCCCGAGCCTCTTGTTGCTGGACTATGACGGGTCGGTG CTGCCCTTCCTCGGGGGCCTGGGCGGGGGCTATCAGA AGACCCTCGTGCTGCTCACCTGGATCCCGGCGCTGTTC ATCGGCTTCAGCCAGTTCTCGGACTCGTTCCTCCTGGA CCAGCCCAACTTCTGGTGCCGCGGGGCCGGCAAAGGC ACCGAGCTGGCAGGGGTCACCACCACAGGCCGGGGC GGGGACATGGGCAACTGGACCAGCCTCCCCACCACCC CCTTCGCCACTGCCCCCTGGGAGGCTGCGGGCAACCG GAGCAACAGCAGCGGCGCGGACGGAGGCGACACACC ACCCCTGCCATCCCCTCCGGACAAGGGGGACAACGCC TCCAACTGTGACTGCCGCGCATGGGACTACGGCATCC GCGCCGGCCTCGTCCAGAACGTGGTCAGCAAGTGGGA TCTTGTGTGTGATAATGCCTGGAAGGTCCATATCGCTA AGTTCTCCTTACTGGTTGGATTAATCTTTGGCTACCTAA TAACTGGATGCATTGCTGACTGGGTCGGCCGGCGGCC TGTGCTGCTGTTTTCCATCATCTTCATTCTGATCTTTGG ACTGACTGTGGCACTGTCAGTGAATGTGACAATGTTCA GCACACTCAGGTTCTTTGAAGGATTTTGCCTGGCTGGA ATCATTCTCACCTTGTATGCTTTAC|GTATCGATATCCT GAAGCTTGTAGCAGCCCAAGTGGGAAGCCAGTGGAA AGATATCTATCAGTTTCTTTGCAATGCCAGTGAGAGGG AGGTTGCTGCTTTCTCCAATGGGTACACAGCCGACCAC GAGCGGGCCTACGCAGCTCTGCAGCACTGGACCATCC GGGGCCCCGAGGCCAGCCTCGCCCAGCTAATTAGCGC CCTGCGCCAGCACCGGAGAAACGATGTTGTGGAGAAG ATTCGTGGGCTGATGGAAGACACCACCCAGCTGGAAA CTGACAAACTAGCTCTCCCGATGagccccagcccgcttagcc cgagccccatccccagccccaacGCGAAACTTGAGAATTCCG CTCTCCTGACGGTGGAGCCTTCCCCACAGGACAAGAAC AAGGGCTTCTTCGTGGATGAGTCGGAGCCCCTTCTCCG CTGTGACTCTACATCCAGCGGCTCCTCCGCGCTGAGCA GGAACGGTTCCTTTATTACCAAAGAAAAGAAGGACAC AGTGTTGCGGCAGGTACGCCTGGACCCCTGTGACTTG CAGCCTATCTTTGATGACATGCTCCACTTTCTAAATCCT GAGGAGCTGCGGGTGATTGAAGAGATTCCCCAGGCTG AGGACAAACTAGACCGGCTATTCGAAATTATTGGAGT CAAGAGCCAGGAAGCCAGCCAGACCCTCCTGGACTCT GTTTATAGCCATCTTCCTGACCTGCTG GBM- 141255367 158715068 InFrame 8363 ATGGAAAACACTG|ATCGAAAAGTATCCTCCTTGCACA CUMC3322_L1 CCTCCCGAGTTCAGAGGCAGATGGTGGTCTCCGTTCAC GACTTACCCGAGAAGAGCTTTGTGCCCCTGCTGGACA GCAAATACGTCCTCTGTGTGTGGGATATTTGGCAGCCT TCAGGGCCACAGAAAGTTCTGATATGTGAGTCCCAGG TCACGTGTTGCTGCTTGAGCCCTTTGAAAGCATTTTTAC TGTTTGCCGGAACAGCGCACGGCTCAGTTGTCGTCTGG GATTTGAGAGAAGACTCAAGGCTGCATTACTCTGTGAC GCTGAGCGATGGCTTCTGGACGTTCCGGACCGCCACG TTTTCCACCGATGGAATCCTTACCTCAGTAAACCACCG AAGCCCTCTTCAAGCAGTAGAACCTATCTCAACGTCCG TCCACAAAAAGCAGAGCTTTGTGCTTTCACCCTTTTCTA CTCAAGAAGAAATGTCAGGTTTGTCCTTCCACATCGCT TCCTTGGATGAGAGTGGGGTTCTCAATGTATGGGTGG TTGTTGAATTACCAAAGGCAGACATCGCAGGTTCAATA AGTGATTTAGGTCTGATGCCTGGAGGGAGGGTCAAGC TGGTACATAGTGCTCTGATCCAGTTGGGTGACAGTCTT TCCCATAAAGGTAATGAATTTTGGGGCACTACACAAAC ACTGAATGTTAAATTTCTGCCTTCAGATCCTAATCACTT TATTATTGGCACAGACATGGGTCTCATAAGCCATGGCA CAAGACAAGATTTGAGAGTGGCTCCCAAACTATTCAAA CCTCAGCAACATGGTATAAGACCAGTGAAAGTTAATGT CATTGATTTTTCACCATTTGGAGAACCAATATTTTTGGC CGGCTGTTCGGACGGAAGCATCAGGCTGCACCAGCTG AGCTCCGCGTTTCCGCTCCTGCAGTGGGACAGCAGCAC GGACAGCCATGCGGTCACCGGCCTGCAGTGGTCCCCA ACCAGGCCTGCCGTGTTCCTGGTGCAGGACGACACAT CCAACATCTACATCTGGGACCTCCTCCAGAGCGATCTG GGTCCTGTCGCCAAACAGCAGGTCTCCCCCAACAGGCT GGTGGCCATGGCTGCGGTGGGTGAGCCTGAGAAGGC TGGTGGCAGCTTCCTGGCCCTGGTGCTGGCCAGGGCG TCTGGCTCCATCGACATCCAGCACCTGAAGAGGCGGT GGGCGGCCCCGGAGGTGGACGAGTGCAACAGGCTGC GTCTGCTTTTGCAGGAAGCCCTGTGGCCAGAGGGAAA ACTGCACAAG G17675. 54379794 56297264 InFrame 8364 ATGACATGCCCTCGCAATGTAACTCCGAACTCGTACGC TCGA-19- GGAGCCCTTGGCTGCGCCCGGCGGAGGAGAGCGCTAT 2624- AGCCGGAGCGCAGGCATGTATATGCAGTCTGGGAGTG 01A-01R- ACTTCAATTGCGGGGTGATGAGGGGCTGCGGGCTCGC 1850- GCCCTCGCTCTCCAAGAGGGACGAGGGCAGCAGCCCC 01.2 AGCCTCGCCCTCAACACCTATCCGTCCTACCTCTCGCAG CTGGACTCCTGGGGCGACCCCAAAGCCGCCTATCGCCT GGAACAACCTGTTGGCAGGCCGCTGTCCTCCTGCTCCT ACCCACCTAGTGTCAAGGAGGAGAATGTCTGCTGCAT GTACAGCGCAGAGAAGCGGGCGAAAAGTGGCCCCGA GGCAGCTCTCTACTCCCACCCCTTGCCGGAGTCCTGCC TTGGGGAGCACGAGGTACCCGTGCCCAGCTACTACCG CGCCAGCCCGAGCTACTCCGCGCTGGACAAGACGCCC CACTGTTCTGGGGCCAACGACTTCGAAGCCCCTTTCGA GCAGCGGGCCAGTCTCAACCCGCGCGCCGAACATCTG GAATCGCCTCAGCTGGGGGGCAAAGTGAGTTTCCCTG AGACCCCCAAGTCCGACAGCCAGACCCCCAGCCCCAAT GAAATCAAGACGGAGCAGAGCCTGGCGGGCCCTAAA GGGAGCCCCTCGGAGAGCGAAAAGGAGAGGGCCAAA GCTGCCGACTCCAGCCCAGACACCTCGGATAACGAAG CGAAAG|GCAAGTATATCGCGTCAACACAGCGACCTG ACGGGACCTGGCGCAAGCAGCGGAGGGTGAAAGAAG GATATGTGCCCCAGGAGGAGGTCCCAGTATATGAAAA CAAGTATGTGAAGTTTTTCAAGAGTAAACCAGAGTTGC CCCCAGGGCTAAGCCCTGAGGCCACTGCTCCTGTCACC CCATCCAGGCCTGAAGGTGGTGAACCAGGCCTCTCCA AGACAGCCAAACGTAACCTGAAGCGAAAGGAGAAGA GGCGGCAGCAGCAAGAGAAAGGAGAGGCAGAGGCCT TGAGCAGGACTCTTGATAAGGTGTCCCTGGAAGAGAC AGCCCAACTCCCCAGTGCTCCACAGGGCTCTCGGGCA GCCCCCACAGCTGCATCTGACCAGCCTGACTCAGCTGC CACCACTGAGAAAGCCAAGAAGATAAAGAACCTAAAG AAGAAACTCCGGCAGGTGGAAGAGCTGCAGCAGCGG ATCCAGGCTGGGGAAGTCAGCCAGCCTAGCAAAGAGC AGCTAGAAAAGCTAGCAAGGAGGAGGGCGCTAGAAG AGGAGTTAGAGGACTTGGAGTTAGGCCTC G17803. 74046509 10694746 InFrame 8365 ATGGCTGCTGAGAAGCAGGTCCCAggcggcggcggcggcg TCGA-76- gcggcagtggcggcggcggtggcagtggcggcggcggtagcggcggt 4925- ggACGTGGTGCCGGAGGGGAAGAAAATAAAGAAAAC 01A-01R- GAACGCCCTTCGGCCGGATCGAAGGCAAACAAAGAAT 1850- TTGGGGATAGCCTGAGTTTGGAGATTCTTCAGATTATT 01.4 AAGGAATCCCAGCAGCAGCATGGTTTACGGCATGGAG ATTTTCAGAGGTACAGGGGCTACTGTTCCCGTAGACAA AGACGTCTTCGAAAAACACTCAACTTCAAGATGGGTAA CAGACACAAATTCACAGGGAAGAAAGTGACTGAAGAG CTTCTGACCGATAATAGATACTTGCTTCTGGTTCTGATG GATGCTGAAAGAGCCTGGAGCTACGCCATGCAGCTGA AACAGGAAGCCAACACTGAACCCCGAAAACGGTTTCA CTTGTTATCTCGCCTACGCAAAGCCGTGAAGCATGCAG AGGAATTGGAACGCTTGTGTGAGAGCAATCGCGTGGA TGCCAAGACCAAATTAGAGGCTCAGGCTTACACAGCTT ACCTCTCAGGAATGCTACGTTTTGAACATCAAGAATGG AAAGCTGCCATTGAGGCTTTTAACAAATGCAAAACTAT CTATGAGAAGCTAGCCAGTGCTTTCACAGAGGAGCAG GCTGTGCTGTATAACCAACGTGTGGAAGAGATTTCACC CAACATCCGCTATTGTGCATATAATATTGGGGACCAGT CAGCCATCAATGAACTCATGCAGATGAGATTGAGGTCT GGGGGCACTGAGGGTCTCTTGGCTGAAAAATTGGAGG CTTTGATCACTCAGACTCGAGCCAAACAGGCAGCTACC ATGAGTGAAGTGGAGTGGAGAGGGAGAACGGTTCCA GTGAAGATTGACAAAGTGCGCATTTTCTTATTAGGACT GGCTGATAACGAAGCAGCTATTGTCCAGGCTGAAAGC GAAGAAACTAAGGAGCGCCTGTTTGAATCAATGCTCA GCGAGTGTCGGGACGCCATCCAGGTGGTTCGGGAGG AGCTCAAGCCAGATCAG|CCATTGATCAGCCGCAACTA CAAGGGCGATGTGGCCATGAGCAAGATTGAGCACTTC ATGCCTTTGCTGGTACAGCGGGAGGAGGAAGGCGCCC TGGCCCCGCTGCTGAGCCACGGCCAGGTCCACTTCCTA TGGATCAAACACAGCAACCTCTACTTGGTGGCCACCAC ATCGAAGAATGCCAATGCCTCCCTGGTGTACTCCTTCC TGTATAAGACAATAGAGGTATTCTGCGAATACTTCAAG GAGCTGGAGGAGGAGAGCATCCGGGACAACTTTGTCA TCGTCTACGAGTTGCTGGACGAGCTCATGGACTTTGGC TTCCCGCAGACCACCGACAGCAAGATCCTGCAGGAGT ACATCACTCAGCAGAGCAACAAGCTGGAGACGGGCAA GTCACGGGTGCCACCCACTGTCACCAACGCTGTGTCCT GGCGCTCCGAGGGTATCAAGTATAAGAAGAACGAGGT CTTCATTGATGTCATAGAGTCTGTCAACCTGCTGGTCA ATGCCAACGGCAGCGTCCTTCTGAGCGAAATCGTCGG TACCATCAAGCTCAAGGTGTTTCTGTCAGGAATGCCAG AGCTGCGGCTGGGCCTCAATGACCGCGTGCTCTTCGA GCTCACTGGCCTTTCAGGCAGCAAGAACAAATCAGTA GAGCTGGAGGATGTAAAATTCCACCAGTGCGTGCGGC TCTCTCGCTTTGACAACGACCGCACCATCTCCTTCATCC CGCCTGATGGTGACTTTGAGCTCATGTCATACCGCCTC AGCACCCAGGTCAAGCCACTGATCTGGATTGAGTCTGT CATTGAGAAGTTCTCCCACAGCCGCGTGGAGATCATG GTCAAGGCCAAGGGGCAGTTTAAGAAACAGTCAGTGG CCAACGGTGTGGAGATATCTGTGCCTGTACCCAGCGAT GCCGACTCCCCCAGATTCAAGACCAGTGTGGGCAGCG CCAAGTATGTGCCGGAGAGAAACGTCGTGATTTGGAG TATTAAGTCTTTCCCGGGGGGCAAGGAGTACTTGATGC GAGCCCACTTTGGCCTCCCCAGTGTGGAAAAGGAAGA GGTGGAGGGCCGGCCCCCCATCGGGGTCAAGTTTGAG ATCCCCTACTTCACCGTCTCTGGGATCCAGGTCCGATA CATGAAGATCATTGAGAAAAGTGGTTACCAGGCCCTG CCCTGGGTTCGCTACATCACCCAGAGTGGCGATTACCA ACTTCGTACCAGC G17796. 58186856 57849877 InFrame 8366 ATGTCGCTGCTGCGGTCGCTGCGCGTGTTTCTGGTCGC TCGA-41- GCGGACCGGGAGCTACCCGGCTGGGTCTCTTCTGCGT 5651- CAGTCGCCCCAGCCAAGGCACACATTTTATGCTGGGCC 01A-01R- CCGTCTGTCTGCCTCGGCCTCCAGCAAGGAGCTCCTCA 1850- TGAAGCTGCGGCGGAAAACAGGCTACTCCTTTGTAAA 01.4 TTGCAAGAAAGCTCTGGAGACTTGTGGCGGGGACCTC AAACAGGCAGAGATCTGGCTCCACAAGGAGGCCCAGA AGGAGGGCTGGAGCAAAGCTGCCAAGCTCCAAGGGA GGAAGACCAAAGAAGGCCTGATTGGGCTGTTGCAGG AAGGAAACACAACTGTATTAGTAGAGGTAAACTGTGA GACAGATTTTGTTTCTAGAAATTTAAAATTTCAACTGTT GGTCCAGCAAGTAGCCCTTGGAACCATGATGCATTGTC AGACCCTAAAGGATCAACCCTCTGCATACAGTAAAgtgc agtggctcacgcctgtaaacctagcactttgggaggctgaagcaggtgg atcacttgagGGTTTCTTGAATTCCTCTGAGCTTTCTGGAC TTCCAGCTGGGCCTGACAGAGAAGGCTCACTCAAGGA TCAGTTGGCTTTAGCAATTG|ACTCCACTTCAGCCTACA GCTCCCTGCTCACTTTTCACCTGTCCACTCCTCGGTCCC ACCACCTGTACCATGCCCGCCTGTGGCTGCACGTGCTC CCCACCCTTCCTGGCACTCTTTGCTTGAGGATCTTCCGA TGGGGACCAAGGAGGAGGCGCCAAGGGTCCCGCACT CTCCTGGCTGAGCACCACATCACCAACCTGGGCTGGCA TACCTTAACTCTGCCCTCTAGTGGCTTGAGGGGTGAGA AGTCTGGTGTCCTGAAACTGCAACTAGACTGCAGACCC CTAGAAGGCAACAGCACAGTTACTGGACAACCGAGGC GGCTCTTGGACACAGCAGGACACCAGCAGCCCTTCCTA GAGCTTAAGATCCGAGCCAATGAGCCTGGAGCAGGCC GGGCCAGGAGGAGGACCCCCACCTGTGAGCCTGCGAC CCCCTTATGTTGCAGGCGAGACCATTACGTAGACTTCC AGGAACTGGGATGGCGGGACTGGATACTGCAGCCCG AGGGGTACCAGCTGAATTACTGCAGTGGGCAGTGCCC TCCCCACCTGGCTGGCAGCCCAGGCATTGCTGCCTCTT TCCATTCTGCCGTCTTCAGCCTCCTCAAAGCCAACAATC CTTGGCCTGCCAGTACCTCCTGTTGTGTCCCTACTGCCC GAAGGCCCCTCTCTCTCCTCTACCTGGATCATAATGGC AATGTGGTCAAGACGGATGTGCCAGATATGGTGGTGG AGGCCTGTGGCTGCAGC G17663. 70800719 94827661 InFrame 8367 ATGGCTTCACTGAGAAGAGTCAAAGTGCTGTTGGTGTT TCGA-19- GAACTTGATCGCGGTAGCCGGCTTCGTGCTCTTCCTGG 2619- CCAAGTGCCGGCCCATCGCGGTGCGCAGCGGAGACGC 01A-01R- CTTCCACGAGATCCGGCCGCGCGCCGAGGTGGCCAAC 1850- CTCAGCGCGCACAGCGCCAGCCCCATCCAGGATGCGG 01.2 TCCTGAAGCGCCTGTCGCTGCTGGAGGACATCGTGTAC CGGCAGCTGAATGGCTTATCCAAATCCCTTGGGCTCAT TGAAGGTTATGGTGGGCGGGGTAAAGGGGGCCTTCC GGCTACTCTTTCCCCGGCTGAAGAAGAAAAGGCTAAG GGACCCCATGAGAAGTATGGCTACAATTCATACCTCAG TGAAAAAATTTCACTGGACCGTTCCATTCCGGATTATC GTCCCACCAA|ATTTGTTATTGGGCGGGAAAAACCAGG ACAAGTGAGCGAGGTTGCCCAGTTGATAAGCCAGACA CTGGAACAGGAGAGGCGCCAGAGAGAGCTGCTGGAA CAGCACTATGCCCAGTATGATGCCGACGATGACGAGA ACACTGTGGCTGAATTGCAAGGAATGTCTGGCAACTG CAATAACAATAACAACTATTTTCTTAAGACAGGAGAAT ATGCCACAGATGAAGAAGAAGATGAGGTAGGACCTGT CCTTCCTGGCAGCGACATGGCCATTGAAGTCTTTGAGC TGCCTGAGAATGAGGACATGTTTTCCCCATCAGAACTG GACACAAGCAAGCTCAGTCACAAGTTCAAAGAGTTGC AAATCAAACATGCAGTTACAGAAGCAGAGATTCAAAA ATTGAAGACCAAGCTGCAGGCAGCAGAAAATGAGAAA GTGAGGTGGGAACTAGAAAAAACCCAACTCCAACAAA ACATAGAAGAGAATAAGGAAAGAATGTTGAAGTTGGA AAGCTACTGGATTGAGGCCCAAACATTATGCCACACA GTGAATGAGCATCTCAAAGAGACTCAAAGCCAGTATC AGGCCTTGGAAAAGAAATACAACAAGGCAAAGAAGTT GATCAAGGATTTTCAACAAAAAGAGCTTGATTTCATCA AAAGACAGGAAGCAGAAAGAAAGAAAATAGAAGATT TGGAAAAAGCTCATCTTGTGGAAGTGCAAGGCCTCCA AGTGCGGATTAGAGATTTGGAAGCTGAGGTATTCAGG CTACTGAAGCAAAATGGGACTCAAGTTAACAATAATAA CAACATCTTTGAGAGAAGAACATCTCTTGGTGAAGTCT CTAAAGGGGATACCATGGAGAACTTGGATGGCAAGCA GACATCTTGCCAAGATGGCCTAAGTCAAGACTTGAATG AAGCAGTCCCAGAGACAGAGCGCCTGGATTCAAAAGC ACTGAAAACTCGAGCCCAGCTCTCTGTGAAGAACAGA CGCCAGAGACCCTCTAGGACAAGACTGTATGATAGTG TTAGTTCCACAGATGGGGAGGACAGTCTAGAGAGAAA GCCATCAAACAGTTTCTATAACCACATGCATATTACCA AATTACTTCCACCTAAGGGTTTGAGAACGTCTTCTCCA GAATCAGATTCTGGTGTTCCACCCCTCACCCCGGTGGA TAGCAATGTGCCCTTCTCGTCTGACCACATAGCTGAAT TTCAAGAAGAACCACTGGACCCAGAAATGGGGCCTCT CTCCTCTATGTGGGGAGACACTTCACTGTTTTCTACTTC AAAGTCTGATCATGATGTGGAAGAATCTCCTTGCCATC ACCAAACCACCAACAAGAAAATATTACGAGAAAAAGA TGATGCCAAAGATCCCAAATCACTAAGGGCATCCAGTT CATTGGCGGTGCAAGGAGGAAAAATTAAGCGGAAGTT TGTGGATCTGGGGGCGCCTTTGCGAAGGAATTCCAGC AAGGGAAAGAAGTGGAAAGAAAAAGAAAAAGAAGCC AGTAGGTTTTCTGCAGGTAGCAGGATCTTCAGAGGCA GACTGGAAAACTGGACACCCAAGCCATGTTCAACAGC TCAGACCTCCACTCGTTCCCCTTGCATGCCTTTCTCATG GTTTAATGACAGCCGGAAAGGATCCTATTCCTTCAGGA ACCTGCCTGCGCCTACAAGTTCCCTTCAGCCTTCTCCTG AGACTCTAATTTCAGATAAAAAGGGGTCCAAGGTAGA AAACACATGGATTACAAAAGCAAACAAGAGAAACCCA AATCCCTCCTCTTCTTCAATCTTTGGAAGGCATTCTCAA CTTATGTCTGTAGTCTGGATCCAAGAAACCAATAATTTT ACCTTCAATGATGACTTCAGTCCCAGCAGTACCAGTTC AGCAGACCTCAGCGGCTTAGGAGCAGAACCTAAAACA CCAGGGCTCTCTCAGTCCTTAGCACTGTCATCAGATGA GATCCTTGATGATGGACAGTCTCCCAAACACAGTCAGT GTCAGAATCGGGCCGTTCAGGAATGGAGTGTGCAGCA GGTTTCTCACTGGTTAATGAGCCTAAATCTGGAGCAGT ATGTATCTGAATTCAGTGCCCAAAACATCACTGGAGAA CAGCTCCTGCAGTTGGATGGAAATAAACTTAAGGCTCT TGGAATGACAGCATCCCAGGACCGAGCAGTGGTCAAA AAGAAACTCAAGGAAATGAAGATGTCTCTAGAGAAGG CTCGGAAGGCCCAAGAGAAAATGGAAAAACAAAGAG AAAAGCTAAGGAGAAAGGAGCAAGAGCAAATGCAGA GGAAGTCCAAAAAGACAGAAAAGATGACGTCAACTAC AGCCGAGGGTGCTGGTGAGCAG G17207. 910775 4438632 InFrame 8368 ATGCAG|AGCACGCAGGCCCATGAGAACAGCAGGGAT TCGA-06- AGCCGGCTGGCATGGATGGGCACCTGGGAGCACCTTG 0156- TGTCTACTGGATTCAACCAGATGCGTGAGCGCGAAGT 01A-03R- GAAGCTGTGGGACACGCGGTTCTTCTCCAGCGCCCTG 1849- GCCTCCCTCACCTTGGACACCTCGCTTGGGTGTCTCGT 01.2 GCCTCTGCTGGACCCTGACTCTGGGCTCCTGGTCCTGG CAGGAAAGGGCGAGAGGCAGCTGTACTGTTACGAGG TGGTCCCGCAGCAGCCGGCGCTGAGCCCAGTGACCCA GTGTGTCCTGGAGAGCGTGCTGCGTGGGGCTGCCCTT GTGCCCCGGCAGGCGCTGGCCGTCATGAGCTGCGAGG TACTCCGCGTCCTACAGCTGAGCGACACAGCCATCGTG CCCATCGGCTACCATGTGCCCCGCAAGGCTGTGGAGTT CCACGAGGACCTGTTCCCGGACACTGCCGGCTGTGTG CCTGCCACCGACCCCCATAGCTGGTGGGCTGGGGACA ACCAGCAGGTGCAGAAGGTCAGCCTCAACCCCGCCTG CCGGCCCCACCCGAGCTTCACTTCCTGTCTGGTGCCCC CTGCGGAGCCCCTCCCTGACACAGCCCAGCCTGCGGT GATGGAGACACCCGTGGGTGATGCAGACGCAAGCGA GGGTTTCTCTTCCCCTCCCAGTTCGCTGACCTCGCCCTC CACGCCCTCCAGCCTGGGGCCCTCACTCTCCAGCACCA GTGGCATCGGGACCAGCCCCAGTTTGAGGTCGCTGCA GAGCCTGCTGGGCCCCAGTTCCAAGTTCCGCCATGCTC AGGGCACTGTCCTGCACCGAGACAGCCACATCACCAA CCTCAAGGGGCTCAACCTCACCACACCTGGTGAGAGT GACGGCTTCTGTGCCAACAAGCTGCGTGTGGCCGTGC CGCTGCTCAGCAGCGGGGGACAGGTGGCTGTGCTTGA GCTACGGAAGCCTGGCCGCCTGCCCGACACGGCACTG CCCACGCTGCAGAATGGGGCAGCTGTGACTGATCTGG CCTGGGACCCCTTTGACCCCCATCGCCTCGCTGTGGCT GGTGAGGACGCCAGGATCCGACTGTGGCGGGTACCC GCAGAGGGCCTGGAAGAGGTGCTCACCACGCCAGAG ACTGTGCTCACAGGCCACACGGAGAAGATCTGCTCCCT GCGCTTCCACCCACTGGCAGCCAATGTGCTGGCCTCGT CCTCCTATGACCTCACTGTTCGCATCTGGGACCTTCAG GCTGGAGCTGATCGGCTGAAGCTGCAGGGCCACCAAG ACCAGATCTTCAGCCTGGCCTGGAGTCCTGATGGGCA GCAGCTGGCCACTGTCTGCAAGGATGGGCGTGTGCGG GTCTACAGGCCCCGGAGTGGCCCTGAGCCCCTGCAGG AAGGCCCAGGGCCCAAGGGAGGACGCGGAGCTCGCA TTGTCTGGGTATGTGATGGTCGCTGTCTGCTGGTGTCT GGCTTTGACAGCCAAAGTGAGCGCCAGCTGCTCCTATA TGAAGCTGAGGCCCTGGCCGGCGGACCCTTGGCAGTG TTGGGCCTGGACGTGGCTCCCTCAACCCTGCTGCCCAG CTACGACCCAGACACTGGCCTGGTGCTCCTGACCGGCA AGGGCGACACCCGTGTATTCCTGTACGAGCTGCTCCCC GAGTCCCCTTTCTTCCTGGAGTGCAACAGCTTCACGTC GCCTGACCCCCACAAGGGCCTCGTCCTCCTGCCTAAGA CGGAGTGCGACGTGCGGGAAGTGGAGCTGATGCGGT GCCTGCGGCTGCGTCAGTCCTCCCTGGAGCCTGTGGCC TTCCGGCTGCCCCGAGTCCGGAAAGAGTTCTTCCAGGA TGACGTGTTCCCAGACACGGCTGTGATCTGGGAGCCT GTGCTCAGTGCCGAGGCCTGGCTGCAAGGCGCTAATG GGCAGCCCTGGCTTCTCAGCCTGCAGCCTCCTGACATG AGCCCAGTGAGCCAAGCCCCCCGAGAGGCCCCTGCTC GTCGGGCCCCATCCTCAGCGCAGTACCTGGAAGAAAA GTCTGACCAGCAAAAGAAGGAGGAGCTGCTGAATGCC ATGGTGGCAAAACTGGGGAACCGGGAGGACCCACTCC CCCAGGACTCCTTTGAAGGCGTGGACGAGGACGAGTG GGAC G17802. 55433922 56079562 InFrame 8369 ATGGGCGAGACCATGTCAAAGAGGCTGAAGCTCCACC TCGA-28- TGGGAGGGGAGGCAGAAATGGAGGAACGGGCGTTCG 5208- TCAACCCCTTCCCGGACTACGAGGCCGCCGCCGGGGC 01A-01R- GCTGCTCGCCTCCGGAGCGGCCGAAGAGACAGGCTGT 1850- GTTCGTCCCCCGGCGACCACGGATGAGCCCGGCCTCCC 01.4 TTTTCATCAGGACGGGAAG|GATGCTTTCATTGGATTT GGAGGAAATGTGATCAGGCAACAAGTCAAGGATAAC GCCAAATGGTATATCACTGATTTTGTAGAGCTGCTGGG AGAACTGGAAGAA G17485. 151216546 151372723 InFrame 8370 ATGCCGCAGTCCAAGTCCCGGAAGATCGCGATCCTGG TCGA-14- GCTACCGGTCTGTGG|CCTCCGGCCTCTCCTCCTCTCCG 1402- TCAACACCCACCCAAGTGACCAAGCAGCACACGTTTCC 02A-01R- CCTGGAATCCTATAAGCACGAGCCTGAACGGTTAGAG 2005- AATCGCATCTATGCCTCGTCTTCCCCCCCGGACACAGG 01.2 GCAGAGGTTCTGCCCGTCTTCCTTCCAGAGCCCGACCA GGCCTCCACTGGCATCACCGACACACTATGCTCCCTCC AAAGCCGCGGCGCTGGCGGCGGCCCTGGGACCCGCG GAAGCCGGCATGCTGGAGAAGCTGGAGTTCGAGGAC GAAGCAGTAGAAGACTCAGAAAGTGGTGTTTACATGC GATTCATGAGGTCACACAAGTGTTATGACATCGTTCCA ACCAGTTCAAAGCTTGTTGTCTTTGATACTACATTACAA GTTAAAAAGGCCTTCTTTGCTTTGGTAGCCAACGGTGT CCGAGCAGCGCCACTGTGGGAGAGTAAAAAACAAAGT TTTGTAGGAATGCTAACAATTACAGATTTCATAAATAT ACTACATAGATACTATAAATCACCTATGGTACAGATTT ATGAATTAGAGGAACATAAAATTGAAACATGGAGGGA GCTTTATTTACAAGAAACATTTAAGCCTTTAGTGAATAT ATCTCCAGATGCAAGCCTCTTCGATGCTGTATACTCCTT GATCAAAAATAAAATCCACAGATTGCCCGTTATTGACC CTATCAGTGGGAATGCACTTTATATACTTACCCACAAA AGAATCCTCAAGTTCCTCCAGCTTTTTATGTCTGATATG CCAAAGCCTGCCTTCATGAAGCAGAACCTGGATGAGC TTGGAATAGGAACGTACCACAACATTGCCTTCATACAT CCAGACACTCCCATCATCAAAGCCTTGAACATATTTGT GGAAAGACGAATATCAGCTCTGCCTGTTGTGGATGAG TCAGGAAAAGTTGTAGATATTTATTCCAAATTTGATGT AATTAATCTTGCTGCTGAGAAAACATACAATAACCTAG ATATCACGGTGACCCAGGCCCTTCAGCACCGTTCACAG TATTTTGAAGGTGTTGTGAAGTGCAATAAGCTGGAAAT ACTGGAGACCATCGTGGACAGAATAGTAAGAGCTGAG GTCCATCGGCTGGTGGTGGTAAATGAAGCAGATAGTA TTGTGGGTATTATTTCCCTGTCGGACATTCTGCAAGCC CTGATCCTCACACCAGCAGGTGCCAAACAAAAGGAGA CAGAAACGGAG NYU_E 88033698 87883123 InFrame 8371 ATGGGTGCTGGGCCCTCCTTGCTGCTCGCCGCCCTCCT GCTGCTTCTCTCCGGCGACGGCGCCGTGCGCTGCGAC ACACCTGCCAACTGCACCTATCTTGACCTGCTGGGCAC CTGGGTCTTCCAGGTGGGCTCCAGCGGTTCCCAGCGC GATGTCAACTGCTCGGTTATGGGACCACAAGAAAAAA AAGTAGTGGTGTACCTTCAGAAGCTGGATACAGCATA TGATGACCTTGGCAATTCTGGCCATTTCACCATCATTTA CAACCAAGGCTTTGAGATTGTGTTGAATGACTACAAGT GGTTTGCCTTTTTTAAGTATAAAGAAGAGGGCAGCAA GGTGACCACTTACTGCAACGAGACAATGACTGGGTGG GTGCATGATGTGTTGGGCCGGAACTGGGCTTGTTTCA CCGGAAAGAAGGTGGGAACTGCCTCTGAGAATGTGTA TGTCAACATAGCACACCTTAAGAATTCTCAGGAAAAGT ATTCTAATAGGCTCTACAAGTATGATCACAACTTTGTG AAAGCTATCAATGCCATTCAGAAGTCTTGGACTGCAAC TACATACATGGAATATGAGACTCTTACCCTGGGAGATA TGATTAGGAGAAGTGGTGGCCACAGTCGAAAAATCCC AAGGCCCAAACCTGCACCACTGACTGCTGAAATACAG CAAAAGATTTTGCATTTGCCAACATCTTGGGACTGGAG AAATGTTCATGGTATCAATTTTGTCAGTCCTGTTCGAAA CCAAG|GTCAAGAAAGATTTGGAAACATGACGAGGGT CTATTACCGAGAAGCTATGGGTGCATTTATTGTCTTCG ATGTCACCAGGCCAGCCACATTTGAAGCAGTGGCAAA GTGGAAAAATGATTTGGACTCCAAGTTAAGTCTCCCTA ATGGCAAACCGGTTTCAGTGGTTTTGTTGGCCAACAAA TGTGACCAGGGGAAGGATGTGCTCATGAACAATGGCC TCAAGATGGACCAGTTCTGCAAGGAGCACGGTTTCGT AGGATGGTTTGAAACATCAGCAAAGGAAAATATAAAC ATTGATGAAGCCTCCAGATGCCTGGTGAAACACATACT TGCAAATGAGTGTGACCTAATGGAGTCTATTGAGCCG GACGTCGTGAAGCCCCATCTCACATCAACCAAGGTTGC CAGCTGCTCTGGCTGTGCCAAATCC G17212. 51128913 42019095 InFrame 8372 ATGGCGGAACGAGGCCTGGAGCCGTCGCCGGCCGCG TCGA-06- GTGGCGGCGCTGCCGCCTGAAGTGCGGGCGCAGCTG 0129- GCGGAGCTGGAGCTGGAGCTCTCGGAGGGGGACATC 01A-01R- ACCCAGAAGGGCTATGAAAAGAAAAGGTCCAAACTCC 1849- TATCTCCTTACAGCCCGCAGACACAAGAAACTGATTCA 01.2 GCAGTACAGAAAGAACTTAGAAACCAGACACCTGCTC CATCTGCAGCTCAAACTTCTGCTCCCTCTAAGTACCACC GAACTCGATCTGGGGGAGCCAGGGATGAACGATATCG ATCAGATATCCACACAGAAGCAGTTCAGGCTGCACTG GCAAAGCATAAAGAACAGAAGATGGCTTTGCCCATGC CAACCAAAAGGCGATCCACATTTGTTCAGTCTCCTGCA GATGCCTGCACACCTCCTGACACATCTTCGGCCTCTGA GGATGAGGGCTCTCTGAGACGCCAAGCTGCGCTCTCT GCTGCCTTGCAACAGAGCTTACAGAATGCTGAGTCCTG GATCAACCGTTCAATTCAGGGATCGTCCACTTCTTCATC CGCATCTTCTACGCTGTCCCACGGAGAGGTCAAAGGA ACCAGTGGGTCTCTAGCTGATGTATTTGCCAATACTCG AATAGAGAATTTCTCTGCTCCTCCTGATGTCACTACAAC TACCTCTTCCTCCTCATCATCTTCCTCAATTCGCCCAGCA AACATTGACCTGCCCCCCTCGGGGATAGTTAAAGGCAT GCACAAAGGATCCAACAGGTCCAGCCTTATGGATACA GCTGATGGTGTTCCTGTCAGTAGCAGAGTATCTACAAA AATCCAGCAGCTTCTGAACACTCTGAAACGACCCAAAA GGCCTCCCTTAAAGGAATTTTTTGTGGATGACTCTGAA GAAATTGTGGAAGTACCTCAGCCAGACCCCAACCAGC CCAAGCCGGAGGGACGGCAGATGACCCCTGTGAAAG GAGAGCCTTTAGGAGTCATCTGTAACTGGCCTCCTGCT CTTGAATCTGCCCTGCAGCGCTGGGGTACCACTCAAGC AAAATGCTCCTGTCTGACTGCACTGGACATGACAGGG AAACCAGTTTACACTCTTACATATGGAAAGTTGTGGAG CAGAAGTTTAAAGTTGGCCTACACACTTCTTAATAAAC TGGGGACCAAAAATGAACCTGTGTTAAAACCTGGAGA CAGGGTAGCCCTGGTTTACCCCAACAATGATCCAGTCA TGTTTATGGTGGCTTTCTATGGATGCCTCCTGGCAGAA GTGATTCCAGTGCCTATAGAGGTACCTCTTACCAGAAA GGATGCTGGAGGTCAGCAGATTGGCTTCTTGCTAGGA AGCTGTGGTATTGCCTTAGCTCTTACCAGTGAAGTTTG TCTAAAAGGACTGCCAAAAACCCAGAATGGAGAAATT GTACAGTTTAAAGGTTGGCCCCGGCTCAAATGGGTTGT AACAGATTCCAAGTACCTTTCAAAGCCACCGAAAGACT GGCAGCCACACATCTCACCTGCTGGGACAGAACCGGC ATACATTGAGTATAAAACAAGCAAAGAAGGGAGTGTA ATGGGAGTTACAGTATCCCGGCTTGCAATGTTGTCTCA CTGCCAAGCTCTGTCGCAGGCCTGCAATTATTCTGAAG GGGAAACAATAGTAAATGTCTTAGACTTTAAGAAGGA TGCTGGGCTGTGGCACGGCATGTTTGCGAATGTAATG AATAAGATGCACACAATCAGCGTACCCTACTCTGTTAT GAAAACCTGTCCTCTCTCTTGGGTCCAAAGAGTACATG CTCACAAAGCCAAGGTAGCTTTAGTAAAATGTCGGGA CTTGCACTGGGCTATGATGGCACATCGGGACCAAAGA GACGTGAGCTTGAGTTCCCTCCGAATGTTAATTGTGAC TGATGGAGCTAACCCCTGGTCCGTGTCATCCTGTGATG CCTTCCTGAGTCTGTTCCAAAGTCATGGACTGAAGCCT GAGGCCATCTGTCCGTGCGCCACGTCTGCTGAAGCCAT GACTGTAGCAATCCGCAGGCCTGGAGTTCCAGGAGCC CCTTTGCCAGGAAGAGCCATTCTCTCAATGAATGGATT GAGCTATGGGGTAATACGGGTCAATACTGAAGATAAA AATTCAGCACTGACGGTCCAGGATGTAGGGCATGTAA TGCCTGGTGGGATGATGTGCATTGTGAAACCAGATGG ACCTCCCCAGCTCTGCAAAACAGATGAAATTGGAGAA ATCTGTGTTAGCTCCAGAACTGGAGGCATGATGTACTT TGGGCTTGCTGGTGTGACAAAAAATACATTTGAGGTA ATTCCAGTGAATTCTGCAGGCTCTCCTGTTGGGGATGT GCCATTCATCCGATCAGGATTGCTGGGGTTTGTAGGGC CGGGTAGTTTGGTGTTCGTGGTTGGGAAAATGGATGG CTTACTGATGGTTAGTGGTCGAAGACATAATGCTGATG ACATTGTTGCTACTGGATTGGCTGTAGAATCAATAAAG ACTGTTTATAGAGGAAGAATTGCTGTGTTTTCTGTGTC TGTATTTTATGATGAGCGCATTGTGGTGGTTGCGGAAC AAAGACCTGATGCTTCTGAGGAAGATAGTTTCCAGTG GATGAGCCGCGTGCTGCAGGCGATCGATAGCATTCAT CAAGTGGGGGTTTATTGTCTTGCTCTGGTGCCAGCCAA TACATTGCCAAAAACTCCACTAGGAGGAATCCATATAT CTCAGACGAAACAACTCTTTCTGGAGGGATCACTGCAT CCTTGCAACATCCTCATGTGCCCCCATACATGTGTGAC AAACTTGCCAAAGCCCCGGCAAAAACAACCAGGTGTA GGCCCTGCTTCCGTGATGGTTGGGAATCTGGTTGCTG GAAAACGTATAGCACAAGCTGCTGGAAGGGATCTGGG ACAAATAGAAGAGAATGATTTGGTGAGGAAGCACCAG TTTCTGGCAGAGATCCTACAGTGGCGAGCCCAGGCGA CTCCTGACCATGTACTCTTCATGCTGTTAAATGCCAAG GGAACCACTGTATGCACAGCCAGCTGCCTTCAGCTTCA TAAGCGAGCAGAGAGGATTGCATCTGTTCTTGGTGAT AAGGGACATCTAAATGCAGGAGATAATGTGGTGTTGC TCTATCCACCTGGCATTGAGTTAATCGCCGCCTTCTATG GCTGCCTGTATGCGGGCTGTATACCTGTGACCGTCAGA CCTCCACATGCTCAGAACCTCACGGCCACGCTGCCCAC TGTCCGAATGATTGTTGATGTCAGCAAAGCAGCCTGTA TTCTCACCAGTCAGACCCTAATGAGGCTACTGAGGTCC CGAGAGGCAGCAGCAGCTGTGGATGTGAAAACCTGG CCAACCATCATTGACACAGATGATTTACCCAGGAAAAG GTTACCTCAGCTGTATAAACCGCCCACTCCTGAGATGT TGGCATATCTTGATTTTAGTGTCTCCACAACTGGCATGC TTACAGGAGTGAAGATGTCCCACTCTGCAGTGAACGCT CTGTGTCGAGCCATCAAGCTCCAGTGTGAGTTGTACTC TTCTCGGCAGATCGCCATCTGCCTTGACCCTTACTGTG GACTTGGCTTCGCGCTCTGGTGTCTCTGCAGTGTCTAT TCAGGCCACCAGTCTGTCTTAATTCCTCCTATGGAGTTA GAGAACAACCTTTTCCTCTGGCTCTCCACAGTCAACCA GTACAAAATAAGGGACACTTTCTGCTCCTATTCAGTGA TGGAGCTCTGCACCAAAGGTCTTGGGAACCAAGTGGA AGTGCTAAAGACCAGAGGGATCAACCTCTCCTGCGTCC GGACCTGTGTGGTGGTGGCGGAGGAGAGGCCCCGCG TTGCACTCCAGCAGTCCTTCTCTAAGCTCTTCAAAGACA TCGGGCTGTCCCCGCGGGCTGTCAGCACCACTTTTGGA TCAAGAGTCAATGTAGCAATATGTTTACAGGGAACCTC AGGGCCTGATCCGACTACTGTGTATGTGGATCTGAAAT CACTAAGACATGACAGGGTTCGTCTCGTGGAACGTGG CGCCCCTCAGAGTTTGCTTCTCTCAGAGTCTGGAAAG| AGATCGGGAAGTAAACAGTCCACTAACCCTGCCGATA ACTATCATCTGGCCCGGAGGAGAACCCTGCAGGTGGT TGTGAGCTCCTTGCTGACAGAGGCAGGGTTTGAGAGT GCCGAGAAAGCATCCGTGGAAACGCTGACAGAGATGC TGCAGAGCTACATTTCAGAAATTGGGAGAAGTGCCAA GTCTTACTGTGAGCACACAGCCAGGACCCAGCCCACAC TGTCCGATATCGTGGTCACACTTGTTGAGATGGGTTTC AATGTGGACACTCTCCCTGCTTATGCAAAACGGTCTCA GAGGATGGTCATCACTGCTCCTCCGGTGACCAATCAGC CAGTGACCCCCAAGGCCCTCACTGCAGGGCAGAACCG ACCCCACCCGCCGCACATCCCCAGCCATTTTCCTGAGTT CCCTGATCCCCACACCTACATCAAAACTCCGACGTACC GTGAGCCCGTGTCAGACTACCAGGTCCTGCGGGAGAA GGCTGCATCCCAGAGGCGCGATGTGGAGCGGGCACTT ACCCGTTTCATGGCCAAGACAGGCGAGACTCAGAGTC TTTTCAAAGATGACGTCAGCACATTTCCATTGATTGCTG CCAGACCTTTCACCATCCCCTACCTGACAGCTCTTCTTC CGTCTGAACTGGAGATGCAACAAATGGAAGAGACAGA TTCCTCGGAGCAGGATGAACAGACAGACACAGAGAAC CTTGCTCTTCATATCAGCATGatagagtctcgctccgtcaccca ggctggagtgcagtggcaagatcttggctcactgcaacctccgcctcct gggttcaagcgattctccagcctcagcctcctgagtagctggaattaca gGAGGATTCTGGAGCCGAGAAGGAGAACACCTCTGTC CTGCAGCAGAACCCCTCCTTGTCGGGTAGCCGGAATG GGGAGGAGAACATCATCGATAACCCTTATCTGCGGCC GG G17787. 13920034 156012704 InFrame 8373 ATGGAACCCCCCGCGGCCAAGCGGAGCCGGGGCTGCC TCGA-26- CCGCGGGACCCGAGGAGCGCGATgccggggccggggccgc 5139- gcgtggccggggccggcccgAGGCGCTGCTGGACCTCAGCG 01A-01R- CCAAGCGGGTAGCCGAGAGCTGGGCCTTCGAGCAGGT 1850- GGAGGAGCGGTTCTCCCGGGTGCCTGAGCCCGTCCAG 01.4 AAGCGCATCGTGTTTTGGTCGTTTCCACGCAGTGAACG GGAAATATGTATGTACTCGTCGCTGGGTTACCCGCCCC CAGAGGGCGAGCACGATGCCCGGGTGCCCTTTACCCG CGGGCTGCACCTGCTCCAGAGCGGGGCCGTGGACCGC GTGTTGCAAGTGGGATTCCACCTGAGCGGAAACATCC GCGAGCCAGGGAGTCCTGGAGAGCCCGAGCGCCTCTA CCATGTCTCCATCAGCTTTGATCGCTGCAAGATCACGT CCGTGAGCTGCGGCTGTGACAACCGCGACCTCTTCTAC TGTGCCCACGTGGTGGCCCTGTCCCTGTACCGCATTCG GCACGCCCACCAGGTGGAGCTGCGGCTGCCCATCTCC GAGACGCTCTCCCAGATGAACCGGGACCAGCTGCAGA AGTTCGTGCAGTACCTCATCAGCGCCCATCACACTGAG GTGCTGCCCACTGCTCAGCGCTTGGCTGATGAGATCCT CCTGCTGGGCTCCGAGATCAACTTGGTGAATGGTGCCC CAGACCCCACCGCCGGCGCAGGAATCGAGGACGCCAA CTGCTGGCACCTGGACGAGGAGCAGATCCAGGAGCA GGTGAAGCAGCTACTGTCCAATGGCGGCTACTACGGG GCCAGCCAGCAGCTGCGCTCCATGTTCAGCAAGGTGC GGGAGATGCTGCGAATGCGGGACTCCAACGGGGCGC GCATGCTGATTCTCATGACCGAGCAGTTCCTGCAGGAC ACGCGCCTGGCCCTGTGGCGGCAGCAGGGCGCGGGC ATGACGGACAAGTGCCGGCAGCTCTGGGATGAGCTGG |GGATGTTCAATAGCCCAGAAATGCAAGCCCTCCTCCA GCAGATCTCTGAGAACCCCCAGCTGATGCAGAATGTG ATCTCAGCACCCTACATGCGCAGCATGATGCAGACGCT TGCCCAGAACCCCGACTTTGCTGCTCAGATGATGGTGA ATGTGCCGCTCTTCGCGGGGAACCCCCAACTGCAGGA GCAGCTCCGCCTGCAGCTCCCAGTCTTCCTGCAGCAGA TGCAGAACCCAGAGTCACTCTCCATCCTTACCAATCCCC GAGCCATGCAGGCATTGCTGCAGATCCAGCAGGGACT ACAGACCTTGCAGACCGAGGCCCCTGGGCTGGTACCC AGCCTTGGCTCCTTTGGGATATCCCGGACCCCAGCACC CTCAGCAGGCAGCAACGCAGGGTCTACGCCCGAGGCC CCCACTTCCTCACCAGCCACGCCAGCCACATCTTCTCCA ACAGGGGCTTCCAGCGCCCAGCAGCAACTCATGCAGC AGATGATCCAGCTTTTGGCTGGAAGTGGAAACTCACA GGTGCAGACGCCAGAAGTGAGATTTCAGCAGCAGCTG GAGCAGCTCAACTCCATGGGCTTCATCAATCGTGAGGC TAACCTGCAGGCCCTGATTGCCACAGGAGGGGACATC AACGCAGCTATCGAGAGACTGCTGGGCTCCCAGCTCTC C G17675. 65232631 63226059 InFrame 8374 ATGGACGTCCTTCCCAccggcgggggccgcccggggcTCCGG TCGA-19- ACGGAGCTGGAATTCCGCGGCGGCGGTGGCGAGGCG 2624- AGGCTGGAGAGTCAGGAGGAAGAAACGATTCCTGCA 01A-01R- GCTCCCCCAGCCCCGCGCCTCCGGGGAGCGGCGGAGC 1850- GGCCGCGGCGCTCCCGGGACACGTGGGACGGCGATG 01.2 AGGACACGGAGCCCGGCGAGGCGTGCGGCGGCCGCA CAAGCCGCACGGCGTCCCTGGTGAGCGGGCTGCTCAA CGAGCTGTACAGCTGCACAGAGGAGGAGGAggcggcgg gcgggggccgcggggccgagggccgccggcggcgccgcgACAGCC TCGACAGCTCCACCGAGGCCTCGGGCTCCGACGTGGT CCTGGGCGGCCGCAGCGGTGCCGGCGACTCCCGCGTG CTGCAGGAGCTGCAGGAGCGACCGAGCCAGCGGCAT CAGATGCTGTACCTGCGGCAGAAAGACGCTAATGAAC TGAAGACGATCCTTCGAGAGCTAAAGTACAGAATTGG CATCCAGTCGGCCAAGTTACTTCGGCATCTGAAGCAGA AAGATAGGCTTCTGCATAAAGTGCAGAGGAACTGTGA TATTGTGACTGCCTGCTTGCAGGCTGTGTCACAGAAGA GAAGAGTTGATACCAAGTTGAAATTCACTCTTGAGCCA TCTTTAGGTCAAAATGGTTTTCAGCAGTGGTACGATGC TCTCAAGGCAGTTGCCAGGCTATCCACAGGAATACCAA AGGAATGGAGGAGAAAGGTTTGGTTGACCTTGGCAG ATCATTATTTGCACAGTATAGCCATTGACTGGGACAAA ACCATGCGCTTCACTTTCAATGAAAGGAGTAATCCTGA TGATGACTCCATGGGAATTCAGATAGTCAAGGACCTTC ACCGCACAGGCTGTAGTTCTTACTGTGGCCAGGAGGC TGAGCAGGACAGGGTTGTGTTGAAGCGGGTGCTGCTG GCCTATGCCCGATGGAACAAAACTGTTGGGTACTGCC AAGGCTTTAACATCCTGGCTGCACTAATTCTGGAAGTG ATGGAAGGCAATGAAGGGGATGCCCTGAAAATTATGA TTTACCTTATTGATAAGGTACTTCCCGAAAGCTATTTCG TCAATAATCTCCGGGCATTGTCTGTGGATATGGCTGTC TTCAGAGACCTTTTAAGAATGAAGCTGCCGGAATTATC TCAGCACCTGGATACTCTTCAGAGAACTGCAAACAAAG AAAGTGGAGGTGGATATGAGCCCCCACTTACAAATGT CTTCACGATGCAGTGGTTTCTGACTCTCTTTGCCACATG CCTCCCTAATCAGACCGTTTTAAAGATCTGGGATTCAG TCTTCTTTGAAGGTTCAGAAATCATCCTAAGGGTGTCG CTGGCTATCTGGGCAAAATTAGGAGA|GGTTATCAAT GCCGGGAAGAGCACACACAATGAAGACCAAGCCAGCT GTGAGGTGCTCACTGTGAAGAAGAAGGCAGGGGCCG TGACCTCAACCCCAAACAGGAACTCATCCAAGAGACG GTCCTCCCTTCCCAATGGGGAAGGGCTGCAGCTGAAG GAGAACTCGGAATCCGAGGGTGTTTCCTGCCACTATTG GTCGCTGTTTGACGGGCACGCGGGGTCCGGGGCCGC GGTGGTGGCGTCACGCCTGCTGCAGCACCACATCACG GAGCAGCTGCAGGACATCGTGGACATCCTGAAGAACT CCGCCGTCCTGCCCCCTACCTGCCTGGGGGAGGAGCCT GAGAACACGCCCGCCAACAGCCGGACTCTGACCCGGG CAGCCTCCCTGCGCGGAGGGGTGGGGGCCCCGGGCTC CCCCAGCACGCCCCCCACACGCTTCTTTACCGAGAAGA AGATTCCCCATGAGTGCCTGGTCATCGGAGCGCTTGAA AGTGCATTCAAGGAAATGGACCTACAGATAGAACGAG AGAGGAGTTCATATAATATATCTGGTGGCTGCACGGC CCTCATTGTGATTTGCCTTTTGGGGAAGCTGTATGTTG CAAATGCTGGGGATAGCAGGGCCATAATCATCAGAAA TGGAGAAATTATCCCCATGTCTTCAGAATTTACCCCCG AGACGGAGCGCCAGCGACTTCAGTACCTGGCATTCAT GCAGCCTCACTTGCTGGGAAATGAGTTCACACATTTGG AGTTTCCAAGGAGAGTACAGAGAAAGGAGCTTGGAA AGAAGATGCTCTACAGGGACTTTAATATGACAGGCTG GGCATACAAAACCATTGAGGATGAGGACTTGAAGTTC CCCCTTATATATGGAGAAGGCAAGAAGGCCCGGGTAA TGGCAACTATTGGAGTGACCAGGGGACTTGGGGACCA TGACCTGAAGGTGCATGACTCCAACATCTACATTAAAC CATTCCTGTCTTCAGCTCCAGAGGTAAGAATCTACGAT CTTTCAAAATATGATCATGGATCAGATGATGTGCTGAT CTTGGCCACTGATGGACTCTGGGACGTTTTATCAAATG AAGAAGTAGCAGAAGCAATCACTCAGTTTCTTCCTAAC TGTGATCCAGATGATCCTCACAGGTACACACTGGCAGC TCAGGACCTGGTGATGCGTGCCCGGGGTGTGCTGAAG GACAGAGGATGGCGGATATCTAATGACCGACTGGGCT CAGGAGACGACATTTCTGTATATGTCATTCCTTTAATAC ATGGAAACAAGCTGTCA G17800. 48586286 56936733 InFrame 8375 ATGGACAATATGTCTATTACGAATACACCAACAAGTAA TCGA-06- TGATGCCTGTCTGAGCATTGTGCATAGTTTGATGTGCC 5859- ATAGACAAGGTGGAGAGAGTGAAACATTTGCAAAAAG 01A-01R- AGCAATTGAAAGTTTGGTAAAGAAGCTGAAGGAGAAA 1849- AAAGATGAATTGGATTCTTTAATAACAGCTATAACTAC 01.4 AAATGGAGCTCATCCTAGTAAATGTGTTACCATACAGA GAACATTGGATGGGAGGCTTCAGGTGGCTGGTCGGAA AGGATTTCCTCATGTGATCTATGCCCGTCTCTGGAGGT GGCCTGATCTTCACAAAAATGAACTAAAACATGTTAAA TATTGTCAGTATGCGTTTGACTTAAAATGTGATAGTGT CTGTGTGAATCCATATCACTACGAACGAGTTGTATCAC CTGGAATTGATCTCTCAGGATTAACACTGCAGAGTAAT GCTCCATCAAGTATGATGGTGAAGGATGAATATGTGC ATGACTTTGAGGGACAGCCATCGTTGTCCACTGAAGG ACATTCAATTCAAACCATCCAGCATCCACCAAGTAATC GTGCATCGACAGAGACATACAGCACCCCAGCTCTGTTA GCCCCATCTGAGTCTAATGCTACCAGCACTGCCAACTT TCCCAACATTCCTGTGGCTTCCACAAGTCAGCCTGCCA GTATACTGGGGGGCAGCCATAGTGAAGGACTGTTGCA GATAGCATCAGGGCCTCAGCCAGGACAGCAGCAGAAT GGATTTACTGGTCAGCCAGCTACTTACCATCATAACAG CACTACCACCTGGACTGGAAGTAGGACTGCACCATAC ACACCTAATTTGCCTCACCACCAAAACGGCCATCTTCA GCACCACCCGCCTATGCCGCCCCATCCCGGACATTACT GGCCTGTTCACAATGAGCTTGCATTCCAGCCTCCCATTT CCAATCATCCTG|GTGTGGTTCCAGAACCGACGGGC G17638. 234299129 234967480 InFrame 8376 ATggcggcggcggcgggcgcccctccgccgggtcccccgcaaccgcct TCGA-28- ccgccgccgccgcccgAGGAGTCGTCCGACAGCGAGCCCG 2499- AGGCGGAGCCCGGCTCCCCACAGAAGCTCATCCGCAA 01A-01R- GGTGTCCACGTCGGGTCAGATCCGACAGAAGACCATC 1850- ATCAAAGAGGGGATGCTGACCAAACAGAACAATTCAT 01.2 TCCAGCGATCAAAAAGGAGATACTTTAAGCTTCGAGG GCGAACGCTTTACTATGCCAAAACGGCAAAGTCAATCA TATTTGATGAGGTGGATCTGACAGATGCCAGCGTAGC TGAATCCAGTACCAAAAACGTCAACAACAGTTTTACG| GTTGAGGTCCTAGATGAGAACAACTTGGTCATGAATTT AGAGTTCAGCATCCGGGAGACTACATGCAGGAAGGAT TCTGGAGAAGATCCCGCTACATGTGCCTTCCAGAGGG ACTACTATGTGTCCACAGCTGTTTGCAGAAGCACCGTG AAGGTATCTGCCCAGCAGGTGCAGGGCGTGCATGCTC GCTGCAGCTGGTCCTCCTCCACGTCTGAGTCTTACAGC AGCGAAGAGATGATTTTTGGGGACATGTTGGGATCTC ATAAATGGAGAAACAATTATCTATTTGGTCTCATTTCA GACGAGTCCATAAGTGAACAATTTTATGATCGGTCACT TGGGATCATGAGAAGGGTATTGCCTCCTGGAAACAGA AGGTACCCAAACCACCGGCACAGAGCAAGAATAAATA CTGACTTTGAG Protein Protein Protein Protein Exon Exon Start Stop Start Stop SEQ ID Break Break sample 5p 5p 3p 3p NO: Protein Sequence 5p 3p G17807. 1 982 190 225 8377 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 6 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 28- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 5209- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01A- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 01R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1850- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.4 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTTYQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HTPPLDPQELDILKTVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSTVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQDAFIGFGGNVI RQQVKDNAKWYITDFVELLGELEE G17197. 1 336 240 432 8378 MGETMSKRLKLHLGGEAEMEERAFVNPFPDY 6 7 TCGA- EAAAGALLASGAAEETGCVRPPATTDEPGLPF 06- HQDGKIIHNFIRRIQTKIKDLLQQMEEGLKTAD 0211- PHDCSAYTGWTGIALLYLQLYRVTCDQTYLLR 01B- SLDYVKRTLRNLNGRRVTFLCGDAGPLAVGAV 01R- IYHKLRSDCESQECVTKLLQLQRSVVCQESDLP 1849- DELLYGRAGYLYALLYLNTEIGPGYVCESAIKEV 01.2 VNAIIESGKTLSREERKTERCPLLYQWHRKQYV GAAHGMAGIYYMLMQPAAKVDQETLTEMV KPSIDYVRHKKFRSGNYPSSLSNETDRLVHWC HGAPGVIHMLMQAYKGLLPFAVVGSTDEVK VGKRMVRGRHYPWGVLQVENENHCDFVKL RDMLLCTNMENLKEKTHTQHYECYRYQKLQK MGFTDVGPNNQPVSFQEIFEAKRQEFYDQC QREEEELKQRFMQRVKEKEATFKEAEKELQDK FEHLKMIQQEEIRKLEEEKKQLEGEIIDFYKMK AASEALQTQLSTDTKKDKHRKK G17650. 1 982 373 432 8379 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 10 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 28- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 2513- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01A- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 01R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1850- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.2 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTTYQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HTPPLDPQELDILKTVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSTVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQLQDKFEHLKMI QQEEIRKLEEEKKQLEGEIIDFYKMKAASEALQ TQLSTDTKKDKHRKK G17506. 1 760 647 838 8380 MGAPACALALCVAVAIVAGASSESLGTEQRV 17 11 TCGA- VGRAAEVPGPEPGQQEQLVFGSGDAVELSCP 27- PPGGGPMGPTVWVKDGTGLVPSERVLVGPQ 1835- RLQVLNASHEDSGAYSCRQRLTQRVLCHFSVR 01A- VTDAPSSGDDEDGEDEAEDTGVDTGAPYWT 01R- RPERMDKKLLAVPAANTVRFRCPAAGNPTPSI 1850- SWLKNGREFRGEHRIGGIKLRHQQWSLVMES 01.2 VVPSDRGNYTCVVENKFGSIRQTYTLDVLERS PHRPILQAGLPANQTAVLGSDVEFHCKVYSDA QPHIQWLKHVEVNGSKVGPDGTPYVTVLKS WISESVEADVRLRLANVSERDGGEYLCRATNF IGVAEKAFWLSVHGPRAAEEELVEADEAGSVY AGILSYGVGFFLFILVVAAVTLCRLRSPPKKGLG SPTVHKISRFPLKRQVSLESNASMSSNTPLVRI ARLSSGEGPTLANVSELELPADPKWELSRARLT LGKPLGEGCFGQVVMAEAIGIDKDRAAKPVT VAVKMLKDDATDKDLSDLVSEMEMMKMIG KHKNIINLLGACTQGGPLYVLVEYAAKGNLREF LRARRPPGLDYSFDTCKPPEEQLTFKDLVSCAY QVARGMEYLASQKCIHRDLAARNVLVTEDNV MKIADFGLARDVHNLDYYKKTTNGRLPVKW MAPEALFDRVYTHQSDVWSFGVLLWEIFTLG GSPYPGIPVEELFKLLKEGHRMDKPANCTHDL YMIMRECWHAAPSQRPTFKQLVEDLDRVLTV TSTDVKATQEENRELRSRCEELHGKNLELGKI MDRFEEVVYQAMEEVQKQKELSKAEIQKVLK EKDQLTTDLNSMEKSFSDLFKRFEKQKEVIEGY RKNEESLKKCVEDYLARITQEGQRYQALKAHA EEKLQLANEEIAQVRSKAQAEALALQASLRKE QMRIQSLEKTVEQKTKENEELTRICDDLISKME KI G17191. 1 336 240 432 8381 MGETMSKRLKLHLGGEAEMEERAFVNPFPDY 6 7 TCGA- EAAAGALLASGAAEETGCVRPPATTDEPGLPF 06- HQDGKIIHNFIRRIQTKIKDLLQQMEEGLKTAD 0211- PHDCSAYTGWTGIALLYLQLYRVTCDQTYLLR 01A- SLDYVKRTLRNLNGRRVTFLCGDAGPLAVGAV 01R- IYHKLRSDCESQECVTKLLQLQRSVVCQESDLP 1849- DELLYGRAGYLYALLYLNTEIGPGTVCESAIKEV 01.2 VNAIIESGKTLSREERKTERCPLLYQWHRKQYV GAAHGMAGIYYMLMQPAAKVDQETLTEMV KPSIDYVRHKKFRSGNYPSSLSNETDRLVHWC HGAPGVIHMLMQAYKGLLPFAVVGSTDEVK VGKRMVRGRHYPWGVLQVENENHCDFVKL RDMLLCTNMENLKEKTHTQHYECYRYQKLQK MGFTDVGPNNQPVSFQEIFEAKRQEFYDQC QREEEELKQRFMQRVKEKEATFKEAEKELQDK FEHLKMIQQEEIRKLEEEKKQLEGEIIDFYKMK AASEALQTQLSTDTKKDKHRKK G17512. 1 982 373 432 8382 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 10 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 27- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 1837- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01A- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 01R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1850- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.2 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTTYQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HTPPLDPQELDILKIVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSTVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQLQDKFEHLKMI QQEEIRKLEEEKKQLEGEIIDFYKMKAASEALQ TQLSTDTKKDKHRKK NYU_A 1 760 548 838 8383 MGAPACALALCVAVAIVAGASSESLGTEQRV 17 8 VGRAAEVPGPEPGQQEQLVFGSGDAVELSCP PPGGGPMGPTVWVKDGTGLVPSERVLVGPQ RLQVLNASHEDSGAYSCRQRLTQRVLCHFSVR VTDAPSSGDDEDGEDEAEDTGVDTGAPYWT RPERMDKKLLAVPAANTVRFRCPAAGNPTPSI SWLKNGREFRGEHRIGGIKLRHQQWSLVMES VVPSDRGNYTCVVENKFGSIRQTYTLDVLERS PHRPILQAGLPANQTAVLGSDVEFHCKVYSDA QPHIQWLKHVEVNGSKVGPDGTPYVTVLKS WISESVEADVRLRLANVSERDGGEYLCRATNF IGVAEKAFWLSVHGPRAAEEELVEADEAGSVY AGILSYGVGFFLFILVVAAVTLCRLRSPPKKGLG SPTVHKISRFPLKRQVSLESNASMSSNTPLVRI ARLSSGEGPTLANVSELELPADPKWELSRARLT LGKPLGEGCFGQVVMAEAIGIDKDRAAKPVT VAVKMLKDDATDKDLSDLVSEMEMMKMIG KHKNIINLLGACTQGGPLYVLVEYAAKGNLREF LRARRPPGLDYSFDTCKPPEEQLTFKDLVSCAY QVARGMEYLASQKCIHRDLAARNVLVTEDNV MKIADFGLARDVHNLDYYKKTTNGRLPVKW MAPEALFDRVYTHQSDVWSFGVLLWEIFTLG GSPYPGIPVEELFKLLKEGHRMDKPANCTHDL YMIMRECWHAAPSQRPTFKQLVEDLDRVLTV TSTDFKESALRKQSLYLKFDPLLRDSPGRPVPV ATETSSMHGANETPSGRPREAKLVEFDFLGAL DIPVPGPPPGVPAPGGPPLSTGPIVDLLQYSQ KDLDAVVKATQEENRELRSRCEELHGKNLELG KIMDRFEEVVYQAMEEVQKQKELSKAEIQKVL KEKDQLTTDLNSMEKSFSDLFKRFEKQKEVIEG YRKNEESLKKCVEDYLARITQEGQRYQALKAH AEEKLQLANEEIAQVRSKAQAEALALQASLRK EQMRIQSLEKTVEQKTKENEELTRICDDLISKM EKI G17814. 1 834 399 796 8384 MARQPPPPWVHAAFLLCLLSLGGAIEIPMDLT 21 10 TCGA- QPPTITKQSAKDHIVDPRDNILIECEAKGNPAP 06- SFHWTRNSRFFNIAKDPRVSMRRRSGTLVIDF 5411- RSGGRPEEYEGEYQCFARNKFGTALSNRIRLQ 01A- VSKSPLWPKENLDPVVVQEGAPLTLQCNPPP 01R- GLPSPVIFWMSSSMEPITQDKRVSQGHNGDL 1849- YFSNVMLQDMQTDYSCNARFHFTHTIQQKN 01.4 PFTLKVLTNHPYNDSSLRNHPDMYSARGVAE RTPSFMYPQGTASSQMVLRGMDLLLECIASG VPTPDIAWYKKGGDLPSDKAKFENFNKALRIT NVSEEDSGEYFCLASNKMGSIRHTISVRVKAA PYWLDEPKNLILAPGEDGRLVCRANGNPKPT VQWMVNGEPLQSAPPNPNREVAGDTIIFRD TQISSRAVYQCNTSNEHGYLLANAFVSVLDVP PRMLSPRNQLIRVILYNRTRLDCPFFGSPIPTLR WFKNGQGSNLDGGNYHVYENGSLEIKMIRKE DQGIYTCVATNILGKAENQVRLEVKDPTRIYR MPEDQVARRGTTVQLECRVKHDPSLKLTVSW LKDDEPLYIGNRMKKEDDSLTIFGVAERDQGS YTCVASTELDQDLAKAYLTVLADQATPTNRLA ALPKGRPDRPRDLELTDLAERSVRLTWIPGDA NNSPITDYVVQFEEDQFQPGVWHDHSKYPG SVNSAVLRLSPYVNYQFRVIAINEVGSSHPSLP SERYRTSGAPPESNPGDVKGEGTRKNNMEIT WTPMNATSAFGPNLRYIVKWRRRETREAWN NVTVWGSRYVVGQTPVYVPYEIRVQAENDFG KGPEPESVIGYSGEDYTNSTSGDPVEKKDETPF GVSVAVGLAVFACLFLSTLLLVLNKCGRRNKF GINRPAVLAPEDGLAMSLHFMTLGGSSLSPTE GKGSGLQGHIIENPQYFSDACVHHIKRRDIVLK WELGEGAFGKVFLAECHNLLPEQDKMLVAVK ALKEASESARQDFQREAELLTMLQHQHIVRFF GVCTEGRPLLMVFEYMRHGDLNRFLRSHGPD AKLLAGGEDVAPGPLGLGQLLAVASQVAAG MVYLAGLHFVHRDLATRNCLVGQGLVVKIGD FGMSRDIYSTDYYRVGGRTMLPIRWMPPESIL YRKFTTESDVWSFGVVLWEIFTYGKQPWYQL SNTEAIDCITQGRELERPRACPPEVYAIMRGC WQREPQQRHSIKDVHARLQALAQAPPVYLD VLG G17223. 1 982 373 432 8385 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 10 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 06- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 0750- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01A- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 01R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1849- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.2 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTTYQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HTPPLDPQELDILKTVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSTVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQLQDKFEHLKMI QQEEIRKLEEEKKQLEGEIIDFYKMKAASEALQ TQLSTDTKKDKHRKK G17798. 1 982 373 432 8386 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 10 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 32- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 5222- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01A- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 01R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1850- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.4 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTTYQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HTPPLDPQELDILKTVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSTVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQLQDKFEHLKMI QQEEIRKLEEEKKQLEGEIIDFYKMKAASEALQ TQLSTDTKKDKHRKK G17195. 1 171 63 246 8387 MFKRMAEFGPDSGGRVKGVTIVKPIVYGNVA 6 2 TCGA- RYFGKKREEDGHTHQWTVYVKPYRNEDMSA 06- YVKKIQFKLHESYGNPLRVVTKPPYEITETGWG 0138- EFEIIIKIFFIDPNERPVTLYHLLKLFQSDTNAML 01A- GKKTVVSEFYDEMIFQDPTAMMQQLLTTSRQ 02R- LTLGAYKHETEYPYVKLLLDAMKHSGCAVNKD 1849- RHFSCEDCNGNVSGGFDASTSQIVLCQNNIH 01.2 NQAHMNRVVTHELIHAFDHCRAHVDWFTNI RHLACSEVRAANLSGDCSLVNEIFRLHFGLKQ HHQTCVRDRATLSILAVRNISKEVAKKAVDEV FESCFNDHEPFGRIPHNKTYARYAHRDFENRD RYYSNI G17803. 1 760 612 838 8388 MGAPACALALCVAVAIVAGASSESLGTEQRV 17 10 TCGA- VGRAAEVPGPEPGQQEQLVFGSGDAVELSCP 76- PPGGGPMGPTVWVKDGTGLVPSERVLVGPQ 4925- RLQVLNASHEDSGAYSCRQRLTQRVLCHFSVR 01A- VTDAPSSGDDEDGEDEAEDTGVDTGAPYWT 01R- RPERMDKKLLAVPAANTVRFRCPAAGNPTPSI 1850- SWLKNGREFRGEHRIGGIKLRHQQWSLVMES 01.4 VVPSDRGNYTCVVENKFGSIRQTYTLDVLERS PHRPILQAGLPANQTAVLGSDVEFHCKVYSDA QPHIQWLKHVEVNGSKVGPDGTPYVTVLKS WISESVEADVRLRLANVSERDGGEYLCRATNF IGVAEKAFWLSVHGPRAAEEELVEADEAGSVY AGILSYGVGFFLFILVVAAVTLCRLRSPPKKGLG SPTVHKISRFPLKRQVSLESNASMSSNTPLVRI ARLSSGEGPTLANVSELELPADPKWELSRARLT LGKPLGEGCFGQVVMAEAIGIDKDRAAKPVT VAVKMLKDDATDKDLSDLVSEMEMMKMIG KHKNIINLLGACTQGGPLYVLVEYAAKGNLREF LRARRPPGLDYSFDTCKPPEEQLTFKDLVSCAY QVARGMEYLASQKCIHRDLAARNVLVTEDNV MKIADFGLARDVHNLDYYKKTTNGRLPVKW MAPEALFDRVYTHQSDVWSFGVLLWEIFTLG GSPYPGIPVEELFKLLKEGHRMDKPANCTHDL YMIMRECWHAAPSQRPTFKQLVEDLDRVLTV TSTDVPGPPPGVPAPGGPPLSTGPIVDLLQYS QKDLDAVVKATQEENRELRSRCEELHGKNLEL GKIMDRFEEVVYQAMEEVQKQKELSKAEIQK VLKEKDQLTTDLNSMEKSFSDLFKRFEKQKEVI EGYRKNEESLKKCVEDYLARITQEGQRYQALK AHAEEKLQLANEEIAQVRSKAQAEALALQASL RKEQMRIQSLEKTVEQKTKENEELTRICDDLIS KMEKI NYU_B 1 31 214 548 8389 MHGGGPPSGDSACPLRTIKRVQFGVLSPDEL 1 5 VPVLRMVEGDTIYDYCWYSLMSSAQPDTSYV ASSSRENPIHIWDAFTGELRASFRAYNHLDELT AAHSLCFSPDGSQLFCGFNRTVRVFSTARPGR DCEVRATFAKKQGQSGIISCIAFSPAQPLYACG SYGRSLGLYAWDDGSPLALLGGHQGGITHLCF HPDGNRFFSGARKDAELLCWDLRQSGYPLWS LGREVTTNQRIYFDLDPTGQFLVSGSTSGAVS VWDTDGPGNDGKPEPVLSFLPQKDCTNGVSL HPSLPLLATASGQRVFPEPTESGDEGEELGLPL LSTRHVHLECRLQLWWCGGAPDSSIPDDHQ GEKGQGGTEGGVGELI G17507. 1 982 373 432 8390 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 10 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 28- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 1747- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01C- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 01R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1850- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.2 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTTYQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HTPPLDPQELDILKIVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSTVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQLQDKFEHLKMI QQEEIRKLEEEKKQLEGEIIDFYKMKAASEALQ TQLSTDTKKDKHRKK G17469. 1 136 980 998 8391 MADFDTYDDRAYSSFGGGRGSRGSAGGHGS 4 34 TCGA- RSQKELPTEPPYTAYVGNLPFNTVQGDIDAIFK 06- DLSIRSVRLVRDKDTDKFKGFCYVEFDEVDSLK 2557- EALTYDGALLGDRSLRVDIAEGRKQDKGGFGF 01A- RKGGPDDREIKETDGSSQIKQEPDPTW 01R- 1849- 01.2 G17785. 1 108 119 239 8392 MLTMSVTLSPLRSQDLDPMATDASPMAINM 2 2 TCGA- TPTVEQGEGEEAMKDMDSDQQYEKPPPLHT 06- GADWKIVLHLPEIETWLRMTSERVRDLTYSVQ 5413- QDSDSKHVDVHLVQLKAMVACYPGNGTGYV 01A- RHVDNPNGDGRCITCIYYLNKNWDAKLHGGI 01R- LRIFPEGKSFIADVEPIFDRLLFFWSDRRNPHEV 1849- QPSYATRYAMTVWYFDAEERAEAKKKFRNLT 01.4 RKTESALTED G17467. 1 83 103 348 8393 MATEGGGKEMNEIKTQFTTREGLYKLLPHSEY 1 3 TCGA- SRPNRVPFNSQGSNPVRVSFVNLNDQSGNG 14- DRLCFNVGRELYFYIYKGVRKEIDPSLGVAELP 0736- DEFFEEDNMLSMGKKMMQEAMSAFPGIDE 02A- AMSYAEVMRLVKGMNFSVVVFDTAPTGHTL 01R- RLLNFPTIVERGLGRLMQIKNQISPFISQMCN 2005- MLGLGDMNADQLASKLEETLPVIRSVSEQFK 01.2 DPEQTTFICVCIAEFLSLYETERLIQELAKCKIDT HNIIVNQLVFPDPEKPCKMCEARHKIQAKYLD QMEDLYEDFHIVKLPLLPHEVRGADKVNTFSA LLLEPYKPPSAQ GBM- 1 164 59 226 8394 MAAAAAAGAGPEMVRGQVFDVGPRYTNLS 3 2 CUMC3316_L1 YIGEGAYGMVCSAYDNVNKVRVAIKKISPFEH QTYCQRTLREIKILLRFRHENIIGINDIIRAPTIEQ MKDVYIVQDLMETDLYKLLKTQHLSNDHICYF LYQILRGLKYIHSANVLHRDLKPSNLLLNTTCDL KALSLCNYFESQNVDFRGKKVIELGAGTGIVGI LAALQGGDVTITDLPLALEQIQGNVQANVPA GGQAQVRALSWGIDHHVFPANYDLVLGADI VYLEPTFPLLLGTLQHLCRPHGTIYLASKMRKE HGTESFFQHLLPQHFQLELAQRDEDENVNIYR ARHREPRPA G17663. 1 876 417 796 8395 MAQLFLPLLAALVLAQAPAALADVLEGDSSED 13 11 TCGA- RAFRVRIAGDAPLQGVLGGALTIPCHVHYLRP 19- PPSRRAVLGSPRVKWTFLSRGREAEVLVARGV 2619- RVKVNEAYRFRVALPAYPASLTDVSLALSELRP 01A- NDSGIYRCEVQHGIDDSSDAVEVKVKGVVFLY 01R- REGSARYAFSFSGAQEACARIGAHIATPEQLY 1850- AAYLGGYEQCDAGWLSDQTVRYPIQTPREAC 01.2 YGDMDGFPGVRNYGVVDPDDLYDVYCYAED LNGELFLGDPPEKLTLEEARAYCQERGAEIATT GQLYAAWDGGLDHCSPGWLADGSVRYPIVT PSQRCGGGLPGVKTLFLFPNQTGFPNKHSRF NVYCFRDSAQPSAIPEASNPASNPASDGLEAI VTVTETLEELQLPQEATESESRGAIYSIPIMEDG GGGSSTPEDPAEAPRTLLEFETQSMVPPTGFS EEEGKALEEEEKYEDEEEKEEEEEEEEVEDEAL WAWPSELSSPGPEASLPTEPAAQEESLSQAPA RAVLQPGASPLPDGESEASRPPRVHGPPTETL PTPRERNLASPSPSTLVEAREVGEATGGPELSG VPRGESEETGSSEGAPSLLPATRAPEGTRELEA PSEDNSGRTAPAGTSVQAQPVLPTDSASRGG VAVVPASGDCVPSPCHNGGTCLEEEEGVRCL CLPGYGGDLCDVGLRFCNPGWDAFQGACYK HFSTRRSWEEAETQCRMYGAHLASISTPEEQ DFINNRYREYQWIGLNDRTIEGDFLWSDGVPL LYENWNPGQPDSYFLSGENCVVMVWHDQG QWSDVPCNYHLSYTCKMGLVSCGPPPELPLA QVFGRPRLRYEVDTVLRYRCREGLAQRNLPLI RCQENGRWEAPQISCVPRRPVSVAVGLAVFA CLFLSTLLLVLNKCGRRNKFGINRPAVLAPEDG LAMSLHFMTLGGSSLSPTEGKGSGLQGHIIEN PQYFSDACVHHIKRRDIVLKWELGEGAFGKVF LAECHNLLPEQDKMLVAVKALKEASESARQD FQREAELLTMLQHQHIVRFFGVCTEGRPLLM VFEYMRHGDLNRFLRSHGPDAKLLAGGEDVA PGPLGLGQLLAVASQVAAGMVYLAGLHFVHR DLATRNCLVGQGLVVKIGDFGMSRDIYSTDYY RVGGRTMLPIRWMPPESILYRKFTTESDVWS FGVVLWEIFTYGKQPWYQLSNTEAIDCITQGR ELERPRACPPEVYAIMRGCWQREPQQRHSIK DVHARLQALAQAPPVYLDVLG G17203. 1 31 336 1210 8396 MDQVMQFVEPSRQFVKDSIRLVKRCTKPDRK 2 9 TCGA- VCNGIGIGEFKDSLSINATNIKHFKNCTSISGDL 06- HILPVAFRGDSFTHTPPLDPQELDILKTVKEITG 0211- FLLIQAWPENRTDLHAFENLEIIRGRTKQHGQ 02A- FSLAVVSLNITSLGLRSLKEISDGDVIISGNKNLC 02R- YANTINWKKLFGTSGQKTKIISNRGENSCKAT 2005- GQVCHALCSPEGCWGPEPRDCVSCRNVSRG 01.2 RECVDKCNLLEGEPREFVENSECIQCHPECLP QAMNITCTGRGPDNCIQCAHYIDGPHCVKTC PAGVMGENNTLVWKYADAGHVCHLCHPNC TYGCTGPGLEGCPTNGPKIPSIATGMVGALLLL LVVALGIGLFMRRRHIVRKRTLRRLLQERELVE PLTPSGEAPNQALLRILKETEFKKIKVLGSGAFG TVYKGLWIPEGEKVKIPVAIKELREATSPKANK EILDEAYVMASVDNPHVCRLLGICLTSIVQLIT QLMPFGCLLDYVREHKDNIGSQYLLNWCVQI AKGMNYLEDRRLVHRDLAARNVLVKTPQHV KITDFGLAKLLGAEEKEYHAEGGKVPIKWMAL ESILHRIYTHQSDVWSYGVTVWELMTFGSKPY DGIPASEISSILEKGERLPQPPICTIDVYMIMVK CWMIDADSRPKFRELIIEFSKMARDPQRYLVI QGDERMHLPSPTDSNFYRALMDEEDMDDV VDADEYLIPQQGFFSSPSTSRTPLLSSLSATSNN STVACIDRNGLQSCPIKEDSFLQRYSSDPTGAL TEDSIDDTFLPVPEYINQSVPKRPAGSVQNPVY HNQPLNPAPSRDPHYQDPHSTAVGNPEYLNT VQPTCVNSTFDSPAHWAQKGSHQISLDNPDY QQDFFPKEAKPNGIFKGSTAENAEYLRVAP QS SEFIGA G17784. 1 150 98 245 8397 MRQSLLFLTSVVPFVLAPRPPDDPGFGPHQRL 4 2 TCGA- EKLDSLLSDYDILSLSNIQQHSVRKRDLQTSTH 76- VETLLTFSALKRHFKLYLTSSTERFSQNFKVVVV 4929- DGKNESEYTVKWQDFFTGHVVGEPDSRVLA 01A- HIRDDDVIIRINTDGAEYNIEELLDKYLIANATN 01R- PESKVFYLKMKGDYFRYLAEVACGDDRKQTID 1850- NSQGAYQEAFDISKKEMQPTHPIRLGLALNFS 01.4 VFYYEILNNPELACTLAKTAFDEAIAELDTLNED SYKDSTLIMQLLRDNLTLWTSDSAGEECDAAE GAEN G17675. 1 228 559 584 8398 MEEDGVRKCKKCEGPCRKVCNGIGIGEFKDSL 14 15 TCGA- SINATNIKHFKNCTSISGDLHILPVAFRGDSFTH 19- TPPLDPQELDILKTVKEITGFLLIQAWPENRTD 2624- LHAFENLEIIRGRTKQQDQTTVSSVPTTLTAPT 01A- ASRPARQESWEKTTPWSGSTQTPAMCATCAI 01R- QTAPTDALGQVLKAVQRMGLRSRPSPLGW 1850- WGPSSCCWWWPWGSASSCEGATSFGSARC 01.2 GGCCRRGRYRFDPRLMFSNRGSVRTRRFSKH LL G17796. 1 96 117 301 8399 MADPGPDPESESESVFPREVGLFADSYSEKSQ 2 3 TCGA- FCFCGHVLTITQNFGSRLGVAARVWDAALSLC 41- NYFESQNVDFRGKKVIELGAGTGIVGILAALQ 5651- VELSPLFPDTLILGLEIRVKVSDYVQDRIRALRA 01A- APAGGFQNIACLRSNAMKHLPNFFYKGQLTK 01R- MFFLFPDPHFKRTKHKWRIISPTLLAEYAYVLR 1850- VGGLVYTITDVLELHDWMCTHFEEHPLFERVP 01.4 LEDLSEDPVVGHLGTSTEEGKKVLRNGGKNFP AIFRRIQDPVLQAVTSQTSLPGH G17666. 1 34 90 300 8400 MVPAAGRRPPRVMRLLGWWQVLLWVLGLP 1 6 TCGA- VRGVEGYNVSLLYDLENLPASKDSIVHQAGML 06- KRNCFASVFEKYFQFQEEGKEGENRAVIHYRD 5415- DETMYVESKKDRVTVVFSTVFKDDDDVVIGK 01A- VFMQEFKEGRRASHTAPQVLFSHREPPLELKD 01R- TDAAVGDNIGYITFVLFPRHTNASARDNTINLI 1849- HTFRDYLHYHIKCSKAYIHTRMRAKTSDFLKVL 01.2 NRARPDAEKKEMKTITGKTFSSR G17219. 1 8 528 926 8401 MDGFAGSLGTLHVGDEIREINGISVANQTVE 1 17 TCGA- QLQKMLREMRGSITFKIVPSYRTQSSSCERDS 06- PSTSRQSPANGHSSTNNSVSDLPSTTQPKGR 0158- QIYVRAQFEYDPAKDDLIPCKEAGIRFRVGDII 01A- QIISKDDHNWWQGKLENSKNGTAGLIPSPEL 01R- QEWRVACIAMEKTKQEQQASCTWFGKKKKQ 1849- YKDKYLAKHNAVFDQLDLVTYEEVVKLPAFKR 01.2 KTLVLLGAHGVGRRHIKNTLITKHPDRFAYPIP HTTRPPKKDEENGKNYYFVSHDQMMQDISN NEYLEYGSHEDAMYGTKLETIRKIHEQGLIAIL DVEPQALKVLRTAEFAPFVVFIAAPTITPGLNE DESLQRLQKESDILQRTYAHYFDLTIINNEIDETI RHLEEAVELVCTAPQWVPVSWVY G17790. 1 23 740 819 8402 MSGQLERCEREWHELEGEFQELQDMKNATL 1 18 TCGA- SLNSNDSEPKYYPIAVLLKNQNQELPEDVNPA 06- KKENYLSEQDFVSVFGITRGQFAALPGWKQL 5856- QMKKEKGLF 01A- 01R- 1849- 01.4 NYU _B 1 93 4035 5204 8403 MGGPQDKDERTIALVRPWPWGHQALDPAY 3 82 GLDTMHPSRRSLPFPLNCQLARVGTADYGSP SDQSDQQLDCALDLMRRLPPQQIEKNLSDLID LDVPVEALTTVKPYCNEIHAQAQLWLKRDPK ASYDAWKKCLPIRGIDGNGKAPSKSELRHLYLT EKYVWRWKQFLSRRGKRTSPLDLKLGHNNW LRQVLFTPATQAARQAACTIVEALATIPSRKQ QVLDLLTSYLDELSIAGECAAEYLALYQKLITSA HWKVYLAARGVLPYVGNLITKEIARLLALEEAT LSTDLQQGYALKSLTGLLSSFVEVESIKRHFKSR LVGTVLNGYLCLRKLVVQRTKLIDETQDMLLE MLEDMTTGTESETKAFMAVCIETAKRYNLDD YRTPVFIFERLCSIIYPEENEVTEFFVTLEKDPQQ EDFLQGRMPGNPYSSNEPGIGPLMRDIKNKIC QDCDLVALLEDDSGMELLVNNKIISLDLPVAE VYKKVWCTTNEGEPMRIVYRMRGLLGDATEE FIESLDSTTDEEEDEEEVYKMAGVMAQCGGL ECMLNRLAGIRDFKQGRHLLTVLLKLFSYCVKV KVNRQQLVKLEMNTLNVMLGTLNLALVAEQ ESKDSGGAAVAEQVLSIMEIILDESNAEPLSED KGNLLLTGDKDQLVMLLDQINSTFVRSNPSVL QGLLRIIPYLSFGEVEKMQILVERFKPYCNFDKY DEDHSGDDKVFLDCFCKIAAGIKNNSNGHQL KDLILQKGITQNALDYMKKHIPSAKNLDADIW KKFLSRPALPFILRLLRGLAIQHPGTQVLIGTDSI PNLHKLEQVSSDEGIGTLAENLLEALREHPDV NKKIDAARRETRAEKKRMAMAMRQKALGTL GMTTNEKGQVVTKTALLKQMEELIEEPGLTCC ICREGYKFQPTKVLGIYTFTKRVALEEMENKPR KQQGYSTVSHFNIVHYDCHLAAVRLARGREE WESAALQNANTKCNGLLPVWGPHVPESAFA TCLARHNTYLQECTGQREPTYQLNIHDIKLLFL RFAMEQSFSADTGGGGRESNIHLIPYIIHTVLY VLNTTRATSREEKNLQGFLEQPKEKWVESAFE VDGPYYFTVLALHILPPEQWRATRVEILRRLLV TSQARAVAPGGATRLTDKAVKDYSAYRSSLLF WALVDLIYNMFKKQTTPTVGGIDTGSLEPCVC EKVPTSNTEGGWSCSLAEYIRHNDMPIYEAAD KALKTFQEEFMPVETFSEFLDVAGLLSEITDPES FLKDLLNSVP G17657. 1 89 39 797 8404 MNGQLDLSGKLIIKAQLGEDIRRIPIHNEDITYD 3 2 TCGA- ELVLMMQRVFRGKLLSNDEVTIKYKDEDGDLI 19- TIFDSSDLSFAIQCSRILKLTLFGKSTSSSSTPTEF 1787- CRNGGTWENGRCICTEEWKGLRCTIANFCEN 01B- STYMGFTFARIPVGRYGPSLQTCGKDTPNAG 01R- NPMAVRLCSLSLYGEIELQKVTIGNCNENLETL 1850- EKQVKDVTAPLNNISSEVQILTSDANKLTAENI 01.2 TSATRVVGQIFNTSRNASPEAKKVAIVTVSQLL DASEDAFQRVAATANDDALTTLIEQMETYSLS LGNQSVVEPNIAIQSANFSSENAVGPSNVRFS VQKGASSSLVSSSTFIHTNVDGLNPDAQTELQ VLLNMTKNYTKTCGFVVYQNDKLFQSKTFTA KSDFSQKIISSKTDENEQDQSASVDMVFSPKY NQKEFQLYSYACVYWNLSAKDWDTYGCQKD KGTDGFLRCRCNHTTNFAVLMTFKKDYQYPK SLDILSNVGCALSVTGLALTVIFQIVTRKVRKTS VTWVLVNLCISMLIFNLLFVFGIENSNKNLQTS DGDINNIDFDNNDIPRTDTINIPNPMCTAIAAL LHYFLLVTFTWNALSAAQLYYLLIRTMKPLPRH FILFISLIGWGVPAIVVAITVGVIYSQNGNNPQ WELDYRQEKICWLAIPEPNGVIKSPLLWSFIVP VTIILISNVVMFITISIKVLWKNNQNLTSTKKVS SMKKIVSTLSVAVVFGITWILAYLMLVNDDSIR IVFSYIFCLFNTTQGLQIFILYTVRTKVFQSEASK VLMLLSSIGRRKSLPSVTRPRLRVKMYNFLRSL PTLHERFRLLETSPSTEEITLSESDNAKESI G17643. 1 20 79 169 8405 MAPARLFALLLFFVGGVAESDYKGQKLAEQM 1 2 TCGA- FQGIILFSAIVGFIYGYVAEQFGWTVYIVMAGF 12- AFSCLLTLPPWPIYRRHPLKWLPVQESSTDDK 5295- KPGERKIKRHAKNN 01A- 01R- 1849- 01.2 NYU_G 1 265 119 974 8406 MRSIRKRWTICTISLLLIFYKTKEIARTEEHQET 4 5 QLIGDGELSLSRSLVNSSDKIIRKAGSSIFQHNV EGWKINSSLVLEIRKNILRFLDAERDVSVVKSSF KPGDVIHYVLDRRRTLNISHDLHSLLPEVSPMK NRRFKTCAVVGNSGILLDSECGKEIDSHNFVIR CNLAPVVEFAADVGTKSDFITMNPSVVQRAF GGFRNESDREKFVHRLSMLNDSVLWIPAFMV KGGEKHVEWVNALILKNKLKVRTAYPSLRLIH AVRGFCDEGTCTDKANILYAWARNAPPTRLP KGVGFRVGGETGSKYFVLQVHYGDISAFRDN NKDCSGVSLHLTRLPQPLIAGMYLMMSVDTV IPAGEKVVNSDISCHYKNYPMHVFAYRVHTH HLGKVVSGYRVRNGQWTLIGRQSPQLPQAFY PVGHPVDVSFGDLLAARCVFTGEGRTEATHIG GTSSDEMCNLYIMYYMEAKHAVSFMTCTQN VAPDMFRTIPPEANIPIPVKSDMVMMHEHH KETEYKDKIPLLQQPKREEEEVLDQGDFYSLLS KLLGEREDVVHVHKYNPTEKAESESDLVAEIA NVVQKKDLGRSDAREGAEHERGNAILVRDRI HKFHRLVSTLRPPESRVFSLQQPPPGEGTWEP EHTGDFHMEEALDWPGVYLLPGQVSGVALD PKNNLVIFHRGDHVWDGNSFDSKFVYQQIGL GPIEEDTILVIDPNNAAVLQSSGKNLFYLPHGL SIDKDGNYWVTDVALHQVFKLDPNNKEGPVL ILGRSMQPGSDQNHFCQPTDVAVDPGTGAIY VSDGYCNSRIVQFSPSGKFITQWGEESSGSSPL PGQFTVPHSLALVPLLGQLCVADRENGRIQCF KTDTKEFVREIKHSSFGRNVFAISYIPGLLFAVN GKPHFGDQEPVQGFVMNFSNGEIIDIFKPVRK HFDMPHDIVASEDGTVYIGDAHTNTVWKFTL TEKLEHRSVKKAGIEVQEIKEAEAVVETKMEN KPTSSELQKMQEKQKLIKEPGSGVPVVLITTLL VIPVVVLLAIAIFIRWKKSRAFGADSEHKLETSS GRVLGRFRGKGSGGLNLGNFFASRKGYSRKG FDRLSTEGSDQEKEDDGSESEEEYSAPLPALAP SSS G17494. 1 85 67 170 8407 MSVDMNSQGSDSNEEDYDPNCEEEEEEEED 1 2 TCGA- DPGDIEDYYVGVASDVEQQGADAFDPEEYQF 14- TCLTYKESEGALNEHMTSLASVLKDGDPDTPK 2554- PVSFTVKETVCPRTTQQSPEDCDFKKDGLVKR 01A- CMGTVTLNQARGSFDISCDKDNKRFALLGDF 01R- FRKSKEKIGKEFKRIVQRIKDFLRNLVPRTES 1850- 01.2 G17196. 1 852 922 995 8408 MSRGAGALQRRTTTYLISLTLVKLESVPPPPPS 13 27 TCGA- PSAAAAGAAGARGSETGDPGSPRGAEEPGKK 06- RHERLFHRQDALWISTSSAGTGGAEPPALSPA 0178- PASPARPVSPAPGRRLSLWAVPPGPPLSGGLS 01A- PDPKPGGAPTSSRRPLLSSPSWGGPEPEGRA 01R- GGGIPGSSSPHPGTGSRRLKVAPPPPAPKPCK 1849- TVTTSGAKAGGGKGAGSRLSWPESEGKPRVK 01.2 GSKSSAGTGASVSAAATAAAAGGGGSTASTS GGVGAGAGARGKLSPRKGKSKTLDNSDLHPG PPAGSPPPLTLPPTPSPATAVTAASAQPPGPA PPITLEPPAPGLKRGREGGRASTRDRKMLKFIS GIFTKSTGGPPGSGPLPGPPSLSSGSGSRELLG AELRASPKAVINSQEWTLSRSIPELRLGVLGDA RSGKSSLIHRFLTGSYQVLEKTESEQYKKEMLV DGQTHLVLIREEAGAPDAKFSGWADAVIFVFS LEDENSFQAVSRLHGQLSSLRGEGRGGLALAL VGTQDRISASSPRVVGDARARALCADMKRCS YYETCATYGLNVDRVFQEVAQKVVTLRKQQQ LLAACKSLPSSPSHSAASTPVAGQASNGGHTS DYSSSLPSSPNVGHRELRAEAAAVAGLSTPGSL HRAAKRRTSLFANRRGSDSEKRSLDSRGETTG SGRAIPIKQSFLLKRSGNSLNKEWKKKYVTLSS NGFLLYHPSINDYIHSTHGKEMDLLRTTVKVP GKRPPRAISAFGPSASINGLVKDMSTVQMGE GLEATTPMPSPSPSPSSLQPPPDQTSKHLLKP DRNLARALSTDCTPSGDLSPLSREPPPSPMVK KQRRKKLTTPSKTEGSAGQAEDEGYSFSSVLYY GNEATLLIFDLLFFCVVDLACQNFILASFLTYLQ QEIFRYIRNTVGQKNLASKTLVDQRFLI G17782. 1 19 140 216 8409 MTHFNKGPSYGLSAEVKNKVLCNGPGTCVPI 1 4 TCGA- CVSALLLGILGIKKVIIVYVESICRVETLSMSGKIL 26- FHLSDYFIVQWPALKEKYPKSVYLGRIV 5136- 01B- 01R- 1850- 01.4 GBM- 1 18 132 179 8410 MRRQPAKVAALLLGLLLEHIEGDDLHIQRNVQ 1 4 CUMC3296_L1 KLKDTVKKLGESGEIKAIGELDLLFMSLRNACI G17199. 1 29 96 406 8411 MRPSGTAGAALLALLAALCPASRALEEKKADI 1 5 TCGA- AQRYRISKYPTLKLFRNGMMMKREYRGQRSV 06- KALADYIRQQKSDPIQEIRDLAEITTLDRSKRNII 0744- GYFEQKDSDNYRVFERVANILHDDCAFLSAFG 01A- DVSKPERYSGDNIIYKPPGHSAPDMVYLGAM 01R- TNFDVTYNWIQDKCVPLVREITFENGEELTEE 1849- GLPFLILFHMKEDTESLEIFQNEVARQLISEKGT 01.2 INFLHADCDKFRHPLLHIQKTPADCPVIAIDSFR HMYVFGDFKDVLIPGKLKQFVFDLHSGKLHRE FHHGPDPTDTAPGEQAQDVASSPPESSFQKL APSEYRYTLLRDRDEL G17792. 1 320 162 453 8412 MTDGKLSTSTNGVAFMGILDGRPGNPLQNL 4 3 TCGA- QHVNLKAPRLLSAPEYGPKLKLRALEDRHSLQ 28- SVDSGIPTLEIGNPEPVPCSAVHVRRKQSDSDL 5204- IPERAFQSACALPSCAPPAPSSTEREQSVRKSS 01A- TFPRTGYDSVKLYSPTSKALTRSDDVSVCSVSS 01R- LGTELSTTLSVSNEDILDLVVTSSSSAIVTLEND 1850- DDPQFTNVTLSSIKETRGLHQQDCVHEAEEGS 01.4 KLKILGPFSNFFARNLLARKQSARLDKHNDLG WKLFGKAPLRENAQKDSKRIQKEYEDKAGRP SKPPSPKQNVRKNLDFEPLSTTALILEDRPAHP LFGRNVPLSSGSGFIMSEAGLIITNAHVVSSNS AAPGRQQLKVQLQNGDSYEATIKDIDKKSDIA TIKIHPKKKLPVLLLGHSADLRPGEFVVAIGSPF ALQNTVTTGIVSTAQREGRELGLRDSDMDYIQ TDAIINYGNSGGPLVNLDGEVIGINTLKVTAGI SFAIPSDRITRFLTEFQDKQIKDWKKRFIGIRM RTITPSLVDELKASNPDFPEVSSGIYVQEVAPN SPSQRGGIQDGDIIVKVNGRPLVDSSELQEAV LTESPLLLEVRRGNDDLLFSIAPEVVM G17476. 1 64 1974 3685 8413 MRLLPRLLLLLLLVFPATVLFRGGPRGLLAVAQ 2 42 TCGA- DLTEDEETVEDSIIEDEDDEAEVEEDEPTDLHT 06- VREETMMVMTEDMPLEISYVPSTYLTEITHVS 2569- QALLEVEQLLNAPDLCAKDFEDLFKQEESLKNI 01A- KDSLQQSSGRIDIIHSKKTAALQSATPVERVKL 01R- QEALSQLDFQWEKVNKMYKDRQGRFDRSVE 1849- KWRRFHYDIKIFNQWLTEAEQFLRKTQIPEN 01.2 WEHAKYKWYLKELQDGIGQRQTVVRTLNAT GEEIIQQSSKTDASILQEKLGSLNLRWQEVCKQ LSDRKKRLEEQKNILSEFQRDLNEFVLWLEEAD NIASIPLEPGKEQQLKEKLEQVKLLVEELPLRQ GILKQLNETGGPVLVSAPISPEEQDKLENKLKQ TNLQWIKVSRALPEKQGEIEAQIKDLGQLEKKL EDLEEQLNHLLLWLSPIRNQLEIYNQPNQEGP FDVKETEIAVQAKQPDVEEILSKGQHLYKEKPA TQPVKRKLEDLSSEWKAVNRLLQELRAKQPDL APGLTTIGASPTQTVTLVTQPVVTKETAISKLE MPSSLMLEVPALADFNRAWTELTDWLSLLDQ VIKSQRVMVGDLEDINEMIIKQKATMQDLEQ RRPQLEELITAAQNLKNKTSNQEARTIITDRIER IQNQWDEVQEHLQNRRQQLNEMLKDSTQW LEAKEEAEQVLGQARAKLESWKEGPYTVDAI QKKITETKQLAKDLRQWQTNVDVANDLALKL LRDYSADDTRKVHMITENINASWRSIHKRVSE REAALEETHRLLQQFPLDLEKFLAWLTEAETTA NVLQDATRKERLLEDSKGVKELMKQWQDLQ GEIEAHTDVYHNLDENSQKILRSLEGSDDAVLL QRRLDNMNFKWSELRKKSLNIRSHLEASSDQ WKRLHLSLQELLVWLQLKDDELSRQAPIGGDF PAVQKQNDVHRAFKRELKTKEPVIMSTLETVR IFLTEQPLEGLEKLYQEPRELPPEERAQNVTRLL RKQAEEVNTEWEKLNLHSADWQRKIDETLER LRELQEATDELDLKLRQAEVIKGSWQPVGDLLI DSLQDHLEKVKALRGEIAPLKENVSHVNDLAR QLTTLGIQLSPYNLSTLEDLNTRWKLLQVAVE DRVRQLHEAHRDFGPASQHFLSTSVQGPWE RAISPNKVPYYINHETQTTCWDHPKMTELYQS LADLNNVRFSAYRTAMKLRRLQKALCLDLLSLS AACDALDQHNLKQNDQPMDILQIINCLTTIYD RLEQEHNNLVNVPLCVDMCLNWLLNVYDTG RTGRIRVLSFKTGIISLCKAHLEDKYRYLFKQVA SSTGFCDQRRLGLLLHDSIQIPRQLGEVASFGG SNIEPSVRSCFQFANNKPEIEAALFLDWMRLE PQSMVWLPVLHRVAAAETAKHQAKCNICKE CPIIGFRYRSLKHFNYDICQSCFFSGRVAKGHK MHYPMVEYCTPTTSGEDVRDFAKVLKNKFRT KRYFAKHPRMGYLPVQTVLEGDNMETPVTLI NFWPVDSAPASSPQLSHDDTHSRIEHYASRLA EMENSNGSYLNDSISPNESIDDEHLLIQHYCQS LNQDSPLSQPRSPAQILISLESEERGELERILADL EEENRNLQAEYDRLKQQHEHKGLSPLPSPPE MMPTSPQSPRDAELIAEAKLLRQHKGRLEAR MQILEDHNKQLESQLHRLRQLLEQPQAEAKV NGTTVSSPSTSLQRSDSSQPMLLRVVGSQTSD SMGEEDLLSPPQDTSTGLEEVMEQLNNSFPSS RGRNTPGKPMREDTM G17195. 1 261 193 667 8414 MPLLGQTVRSASARTRRWSRRAAGDRPGAP 6 6 TCGA- SEARRPQLRGDHGIVDRVRGHWRIAGSCSTC 06- WCPSALCSSTNGFMCTFPNMSLTLVHFVVT 0138- WLGLYICQKLDIFAPKSLPPSRLLLLALSFCGFV 01A- VFTNLSLQNNTIGTYQLAKAMTTPVIIAIQTFC 02R- YQKTFSTRIQLTLIPITLGVILNSYYDVKFNFLG 1849- MVFAALGVLVTSLYQVWVGAKQHELQVNS 01.2 MQLLYYQAPMSSAMLLVAVPFFEPVFGEGGI FGPWSVSALFLCDEGAGISGDYIDRVDEPLSCS YVLTIRTPRLCPHPLLRPPPSAAPQAILCHPSLQ PEEYMAYVQRQADSKQYGDKIIEELQDLGPQ VWSETKSGVAPQKMAGASPTKDDSKDSDFW KMLNEPEDQAPGGEEVPAEEQDPSPEAADSA SGAPNDFQNNVQVKVIRSPADLIRFIEELKGG TKKGKPNIGQEQPVDDAAEVPQREPEKERGD PERQREMEEEEDEDEDEDEDEDERQLLGEFE KELEGILLPSDRDRLRSEVKAGMERELENIIQET EKELDPDGLKKESERDRAMLALTSTLNKLIKRL EEKQSPELVKKHKKKRVVPKKPPPSPQPTEED PEHRVRVRVTKLRLGGPNQDLTVLEMKRENP QLKQIEGLVKELLEREGLTAAGKIEIKIVRPWAE GTEEGARWLTDEDTRNLKEIFFNILVPGAEEA QKERQRQKELESNYRRVWGSPGGEGTGDLD EFDF G17212. 1 810 134 341 8415 MVPEAWRSGLVSTGRVVGVLLLLGALNKAST 1 4 TCGA- VIHYEIPEEREKGFAVGNVVANLGLDLGSLSAR 06- RFRVVSGASRRFFEVNRETGEMFVNDRLDRE 0129- ELCGTLPSCTVTLELVVENPLELFSVEVVIQDIN 01A- DNNPAFPTQEMKLEISEAVAPGTRFPLESAHD 01R- PDVGSNSLQTYELSRNEYFALRVQTREDSTKY 1849- AELVLERALDREREPSLQLVLTALDGGTPALSA 01.2 SLPIHIKVLDANDNAPVFNQSLYRARVLEDAPS GTRVVQVLATDLDEGPNGEIIYSFGSHNRAGV RQLFALDLVTGMLTIKGRLDFEDTKLHEIYIQA KDKGANPEGAHCKVLVEVVDVNDNAPEITVT SVYSPVPEDAPLGTVIALLSVTDLDAGENGLVT CEVPPGLPFSLTSSLKNYFTLKTSADLDRETVPE YNLSITARDAGTPSLSALTIVRVQVSDINDNPP QSSQSSYDVYIEENNLPGAPILNLSVWDPDAP QNARLSFFLLEQGAETGLVGRYFTINRDNGIVS SLVPLDYEDRREFELTAHISDGGTPVLATNISV NIFVTDRNDNAPQVLYPRPGGSSVEMLPRGT SAGHLVSRVVGWDADAGHNAWLSYSLLGSP NQSLFAIGLHTGQISTARPVQDTDSPRQTLTV LIKDNGEPSLSTTATLTVSVTEDSPEARAEFPSG SAPREQKKNLTFYLLLSLILVSVGFVVTVEGVIIF KVYKWKQSRDLYRAPVSSLYRTPGPSLHADAV RGGLMSPHLYHQVYLTTDSRRSDPLLKKPGAA SPLASRQNTLRSCDPVFYRQVLGAESAPPGQE EQNRGKPNWEHLNEDLHVLITVEDAQNRAEI KLKRAVEEVKKLLVPAAEGEDSLKKMQLMELA ILNGTYRDANIKSPALAFSLAATAQAAPRIITGP APVLPPAALRTPTPAGPTIMPLIRQIQTAVMP NGTPHPTAAIVPPGPEAGLIYTPYEYPYTLAPA TSILEYPIEPSGVLGAVATKVRRHDMRVHPYQ RIVTADRAATGN G17213. 1 12 131 278 8416 MADIEQYYMKPPEIVKEAEVPQAALGVPAQG 2 2 TCGA- TGDNGHTPVEEEVGGIPVPAPGLLQVTERRQ 06- PLSSVSSLEVHFDLLDLTELTDMSDQELAEVFA 0157- DSDDENLNTESPAGLHPLPRAGYLRSPSWTRT 01A- RAEQSHEKQPLGDPERQAIVLDTFLTVERPQE 01R- D 1849- 01.2 G17200. 1 1066 710 1072 8417 MAAQVAPAAASSLGNPPPPPPSELKKAEQQQ 11 12 TCGA- REEAGGEAAAAAAAERGEMKAAAGQESEGP 06- AVGPPQPLGKELQDGAESNGGGGGGGAGSG 0125- GGPGAEPDLKNSNGNAGPRPALNNNLTEPP 01A- GGGGGGSSDGVGAPPHSAAAALPPPAYGFG 01R- QPYGRSPSAVAAAAAAVFHQQHGGQQSPGL 1849- AALQSGGGGGLEPYAGPQQNSHDHGFPNH 01.2 QYNSYYPNRSAYPPPAPAYALSSPRGGTPGSG AAAAAGSKPPPSSSASASSSSSSFAQQRFGAM GGGGPSAAGGGTPQPTATPTLNQLLTSPSSA RGYQGYPGGDYSGGPQDGGAGKGPADMAS QCWGAAAAAAAAAAASGGAQQRSHHAPM SPGSSGGGGQPLARTPQPSSPMDQMGKMR PQPYGGTNPYSQQQGPPSGPQQGHGYPGQ PYGSQTPQRYPMTMQGRAQSAMGGLSYTQ QIPPYGQQGPSGYGQQGQTPYYNQQSPHPQ QQQPPYSQQPPSQTPHAQPSYQQQPQSQPP QLQSSQPPYSQQPSQPPHQQSPAPYPSQQST TQQHPQSQPPYSQPQAQSPYQQQQPQQPA PSTLSQQAAYPQPQSQQSQQTAYSQQRFPPP QELSQDSFGSQASSAPSMTSSKGGQEDMNLS LQSRPSSLPDLSGSIDDLPMGTEGALSPGVSTS GISSSQGEQSNPAQSPFSPHTSPHLPGIRGPSP SPVGSPASVAQSRSGPLSPAAVPGNQMPPRP PSGQSDSIMHPSMNQSSIAQDRGYMQRNPQ MPQYSSPQPGSALSPRQPSGGQIHTGMGSY QQNSMGSYGPQGGQYGPQGGYPRQPNYN ALPNANYPSAGMAGGINPMGAGGQMHGQ PGIPPYGTLPPGRMSHASMGNRPYGPNMAN MPPQVGSGMCPPPGGMNRKTQETAVAMH VAANSIQNRPPGYPNMNQGGMMGTGPPY GQGINSMAGMINPQGPPYSMGGTMANNSA GMAASPEMMGLGDVKLTPATKMNNKADGT PKTESKSKKSSSSTTTNEKITKLYELGGEPERKM WVDRYLAFTEEKAMGMTNLPAVGRKPLDLY RLYVSVKEIGGLTQMQALTSCECTICPDCFRQ HFTIALKEKHITDMVCPACGRPDLTDDTQLLS YFSTLDIQLRESLEPDAYALFHKKLTEGVLMRD PKFLWCAQCSFGFIYEREQLEATCPQCHQTFC VRCKRQWEEQHRGRSCEDFQNWKRMNDPE YQAQGLAMYLQENGIDCPKCKFSYALARGGC MHFHCTQCRHQFCSGCYNAFYAKNKCPEPN CRVKKSLHGHHPRDCLFYLRDWTALRLQKLLQ DNNVMFNTEPPAGARAVPGGGCRVIEQKEV PNGLRDEACGKETPAGYAGLCQAHYKEYLVSL INAHSLDPATLYEVEELETATERYLHVRPQPLA GEDPPAYQARLLQKLTEEVPLGQSIPRRRK G17804. 1 982 190 225 8418 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 6 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 06- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 5408- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01A- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 01R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1849- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.4 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTPQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HIPPLDPQELDILKTVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSIVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQDAFIGFGGNVI RQQVKDNAKWYITDFVELLGELEE G17656. 1 379 298 421 8419 MAAQVAPAAASSLGNPPPPPPSELKKAEQQQ 1 5 TCGA- REEAGGEAAAAAAAERGEMKAAAGQESEGP 28- AVGPPQPLGKELQDGAESNGGGGGGGAGSG 2514- GGPGAEPDLKNSNGNAGPRPALNNNLTEPP 01A- GGGGGGSSDGVGAPPHSAAAALPPPAYGFG 02R- QPYGRSPSAVAAAAAAVFHQQHGGQQSPGL 1850- AALQSGGGGGLEPYAGPQQNSHDHGFPNH 01.2 QYNSYYPNRSAYPPPAPAYALSSPRGGTPGSG AAAAAGSKPPPSSSASASSSSSSFAQQRFGAM GGGGPSAAGGGTPQPTATPTLNQLLTSPSSA RGYQGYPGGDYSGGPQDGGAGKGPADMAS QCWGAAAAAAAAAAASGGAQQRSHHAPM SPGSSGGGGQPLARTPQVHLGSGIWVDEEK WHQLQVTQGDSKYTKNLAVMIWGTDVLKN RSVTGVATKKKKDAVPKPPLSPHKLSIVRECLY DRIAQETVDETEIAQRLSKVNKYICEKIMDINK SCKNEERREAKYNLQ G17654. 1 329 102 545 8420 MLLSLPALHLQTSEHHPFFQLPHRRLGPWCSP 7 6 TCGA- TGSPAPLSCETGCGEGSWILVCRLLVPTQVSLL 41- SMEEDIDTRKINNSFLRDHSYATEADIISTVEFN 4097- HTGELLATGDKGGRVVIFQREQESKNQVHRR 01A- GEYNVYSTFQSHEPEFDYLKSLEIEEKINKIRWL 01R- PQQNAAYFLLSTNDKTVKLWKVSERDKRPEG 1850- YNLKDEEGRLRDPATITTLRVPVLRPMDLMVE 01.2 ATPRRVFANAHTYHINSISVNSDYETYMSADD LRINLWNFEITNQSFNIVDIKPANMEELTEVIT AAEFHPHHCNTFVYSSSKGTIRLCDMRASALC DRHTKSGEMLSVAEHFLEQQMHPTVVISAYR KALDDMISTLKKISIPVDISDSDMMLNIINSSIT TKAISRWSSLACNIALDAVKMVQFEENGRKEI DIKKYARVEKIPGGIIEDSCVLRGVMINKDVTH PRMRRYIKNPRIVLLDSSLEYKKGESQTDIEITR EEDFTRILQMEEEYIQQLCEDIIQLKPDVVITEK GISDLAQHYLMRANITAIRRVRKTDNNRIARA CGARIVSRPEELREDDVGTGAGLLEIKKIGDEY FTFITDCKDPKACTILLRGASKEILSEVERNLQD AMQVCRNVLLDPQLVPGGGASEMAVAHALT EKSKAMTGVEQWPYRAVAQALEVIPRTLIQN CGASTIRLLTSLRAKHTQENCETWGVNGETGT LVDMKELGIWEPLAVKLQTYKTAVETAVLLLRI DDIVSGHKKKGDDQSRQGGAPDAGQE G17206. 1 1066 710 1072 8421 MAAQVAPAAASSLGNPPPPPPSELKKAEQQQ 11 12 TCGA- REEAGGEAAAAAAAERGEMKAAAGQESEGP 06- AVGPPQPLGKELQDGAESNGGGGGGGAGSG 0125- GGPGAEPDLKNSNGNAGPRPALNNNLTEPP 02A- GGGGGGSSDGVGAPPHSAAAALPPPAYGFG 11R- QPYGRSPSAVAAAAAAVFHQQHGGQQSPGL 2005- AALQSGGGGGLEPYAGPQQNSHDHGFPNH 01.2 QYNSYYPNRSAYPPPAPAYALSSPRGGTPGSG AAAAAGSKPPPSSSASASSSSSSFAQQRFGAM GGGGPSAAGGGTPQPTATPTLNQLLTSPSSA RGYQGYPGGDYSGGPQDGGAGKGPADMAS QCWGAAAAAAAAAAASGGAQQRSHHAPM SPGSSGGGGQPLARTPQPSSPMDQMGKMR PQPYGGTNPYSQQQGPPSGPQQGHGYPGQ PYGSQTPQRYPMTMQGRAQSAMGGLSYTQ QIPPYGQQGPSGYGQQGQTPYYNQQSPHPQ QQQPPYSQQPPSQTPHAQPSYQQQPQSQPP QLQSSQPPYSQQPSQPPHQQSPAPYPSQQST TQQHPQSQPPYSQPQAQSPYQQQQPQQPA PSTLSQQAAYPQPQSQQSQQTAYSQQRFPPP QELSQDSFGSQASSAPSMTSSKGGQEDMNLS LQSRPSSLPDLSGSIDDLPMGTEGALSPGVSTS GISSSQGEQSNPAQSPFSPHTSPHLPGIRGPSP SPVGSPASVAQSRSGPLSPAAVPGNQMPPRP PSGQSDSIMHPSMNQSSIAQDRGYMQRNPQ MPQYSSPQPGSALSPRQPSGGQIHTGMGSY QQNSMGSYGPQGGQYGPQGGYPRQPNYN ALPNANYPSAGMAGGINPMGAGGQMHGQ PGIPPYGTLPPGRMSHASMGNRPYGPNMAN MPPQVGSGMCPPPGGMNRKTQETAVAMH VAANSIQNRPPGYPNMNQGGMMGTGPPY GQGINSMAGMINPQGPPYSMGGTMANNSA GMAASPEMMGLGDVKLTPATKMNNKADGT PKTESKSKKSSSSTTTNEKITKLYELGGEPERKM WVDRYLAFTEEKAMGMTNLPAVGRKPLDLY RLYVSVKEIGGLTQMQALTSCECTICPDCFRQ HFTIALKEKHITDMVCPACGRPDLTDDTQLLS YFSTLDIQLRESLEPDAYALFHKKLTEGVLMRD PKFLWCAQCSFGFIYEREQLEATCPQCHQTFC VRCKRQWEEQHRGRSCEDFQNWKRMNDPE YQAQGLAMYLQENGIDCPKCKFSYALARGGC MHFHCTQCRHQFCSGCYNAFYAKNKCPEPN CRVKKSLHGHHPRDCLFYLRDWTALRLQKLLQ DNNVMFNTEPPAGARAVPGGGCRVIEQKEV PNGLRDEACGKETPAGYAGLCQAHYKEYLVSL INAHSLDPATLYEVEELETATERYLHVRPQPLA GEDPPAYQARLLQKLTEEVPLGQSIPRRRK G17792. 1 161 121 238 8422  MAELDPFGAPAGAPGGPALGNGVAGAGEED 4 4 TCGA- PAAAFLAQQESEIAGIENDEAFAILDGGAPGP 28- QPHGEPPGGPDAVDGVMNGEYYQESNGPT 5204- DSYAAISQVDRLQSEPESIRKWREEQMERLEA 01A- LDANSRKQEAEWKEKAIKELEEWYARQDEQL 01R- QKTKANNRTILLSVISLLNEPNTFSPANVDASV 1850- MFRKWRDSKGKDKEYAEIIRKQVSATKAEAEK 01.4 DGVKVPTTLAEYCIKTKVPSNDNSSDLLYDDLY DDDIDDEDEEEEDADCYDDDDSGNEES G17663. 1 5 322 502 8423  MSRPVRFMERNPLTNAIIRTTTALTIFKAGVKF 1 9 TCGA- NVIPPVAQATVNFRIHPGQTVQEVLELTKNIV 19- ADNRVQFHVLSAFDPLPVSPSDDKALGYQLLR 2619- QTVQSVFPEVNITAPVTSIGNTDSRFFTNLTTG 01A- IYRFYPIYIQPEDFKRIHGVNEKISVQAYETQVK 01R- FIFELIQNADTDQEPVSHLHKL 1850- 01.2 NYU_E 1 510 7 437 8424  MRVAAATAAAGAGPAMAVWTRATKAGLVE 6 2 LLLRERWVRVVAELSGESLSLTGDAAAAELEP ALGPAAAAFNGLPNGGGAGDSLPGSPSRGLG PPSPPAPPRGPAGEAGASPPVRRVRVVKQEA GGLGISIKGGRENRMPILISKIFPGLAADQSRAL RLGDAILSVNGTDLRQATHDQAVQALKRAGK EVLLEVKFIREVTPYIKKPSLVSDLPWEGAAPQ SPSFSGSEDSGSPKHQNSTKDRKIIPLKMCFAA RNLSMPDLENRLIELHSPDSRNTLILRCKDTAT AHSWFVAIHTNIMALLPQVLAELNAMLGATS TAGGSKEVKHIAWLAEQAKLDGGRQQWRPV LMAVTEKDLLLYDCMPWTRDAWASPCHSYP LVATRLVHSGSGCRSPSLGSDLTFATRTGSRQ GIEMHLFRVETHRDLSSWTRILVQGCHAAAEL IKEVSLGCMLNGQEVRLTIHYENGFTISRENG GSSSILYRYPFERLKMSADDGIRNLYLDFGGPE GELKAIDLVTKATEEDKAKNYEEALRLYQHAVE YFLHAIKYEAHSDKAKESIRAKCVQYLDRAEKL KDYLRSKEKHGKKPVKENQSEGKGSDSDSEG DNPEKKKLQEQLMGAVVMEKPNIRWNDVA GLEGAKEALKEAVILPIKFPHLFTGKRTPWRGIL LFGPPGTGKSYLAKAVATEANNSTFFSVSSSDL MSKWLGESEKLVKNLFELARQHKPSIIFIDEVD SLCGSRNENESEAARRIKTEFLVQMQGVGNN NDGTLVLGATNIPWVLDSAIRRRFEKRIYIPLPE EAARAQMFRLHLGSTPHNLTDANIHELARKTE GYSGADISIIVRDSLMQPVRKVQSATHFKKVC GPSRTNPSMMIDDLLTPCSPGDPGAMEMT WMDVPGDKLLEPVVCMSDMLRSLATTRPTV NADDLLKVKKFSEDFGQES NYU_G 1 7 95 483 8425 MKTPADTGDSGKVTTVVATLGQGPERSQEV 1 2 AYTDIKVIGNGSFGVVYQARLAETRELVAIKKV LQDKRFKNRELQIMRKLDHCNIVRLRYFFYSSG EKKDELYLNLVLEYVPETVYRVARHFTKAKLTIP ILYVKVYMYQLFRSLAYIHSQGVCHRDIKPQNL LVDPDTAVLKLCDFGSAKQLVRGEPNVSYICS RYYRAPELIFGATDYTSSIDVWSAGCVLAELLL GQPIFPGDSGVDQLVEIIKVLGTPTREQIREM NPNYTEFKFPQIKAHPWTKVEKSRTPPEAIALC SSLLEYTPSSRLSPLEACAHSFFDELRCLGTQLP NNRPLPPLFNFSAGELSIQPSLNAILIPPHLRSP AGTTTLTPSSQALTETPTSSDWQSTDATPTLT NSS NYU_B 1 602 13 455 8426 MGMARGSLTRVPGVMGEGTQGPELSLDPDP 11 2 CSPQSTPGLMKGNKLEEQDPRPLQPIPGLME GNKLEEQDSSPPQSTPGLMKGNKREEQGLGP EPAAPQQPTAEEEALIEFHRSYRELFEFFCNNT TIHGAIRLVCSQHNRMKTAFWAVLWLCTFG MMYWQFGLLFGEYFSYPVSLNINLNSDKLVFP AVTICTLNPYRYPEIKEELEELDRITEQTLFDLYK YSSFTTLVAGSRSRRDLRGTLPHPLQRLRVPPP PHGARRARSVASSLRDNNPQVDWKDWKIGF QLCNQNKSDCFYQTYSSGVDAVREWYRFHYI NILSRLPETLPSLEEDTLGNFIFACRFNQVSCN QANYSHFHHPMYGNCYTFNDKNNSNLWMS SMPGINNGLSLMLRAEQNDFIPLLSTVTGARV MVHGQDEPAFMDDGGFNLRPGVETSISMRK ETLDRLGGDYGDCTKNGSDVPVENLYPSKYT QQVCIHSCFQESMIKECGCAYIFYPRPQNVEY CDYRKHSSWGYCYYKLQVDFSSDHLGCFTKCR KPCSVTSYQLSAGYSRWPSVTSQEWVFQMLS RQNNYTVNNKRNGVAKVNIFFKELNYKTNSE SPSVTVLLELLVGIYPSGVIGLVPHLGDREKRDS VCPQGKYIHPQNNSICCTKCHKGTYLYNDCPG PGQDTDCRECESGSFTASENHLRHCLSCSKCR KEMGQVEISSCTVDRDTVCGCRKNQYRHYW SENLFQCFNCSLCLNGTVHLSCQEKQNTVCTC HAGFFLRENECVSCSNCKKSLECTKLCLPQIEN VKGTEDSGTTVLLPLVIFFGLCLLSLLFIGLMYR YQRWKSKLYSIVCGKSTPEKEGELEGTTTKPLA PNPSFSPTPGFTPTLGFSPVPSSTFTSSSTYTPG DCPNFAAPRREVAPPYQGADPILATALASDPI PNPLQKWEDSAHKPQSLDTDDPATLYAVVEN VPPLRWKEFVRRLGLSDHEIDRLELQNGRCLR EAQYSMLATWRRRTPRREATLELLGRVLRDM DLLGCLEDIEEALCGPAALPPAPSLLR G17675. 1 306 137 514 8427 MVRSRQMCNTNMSVPTDGAVTTSQIPASEQ 10 3 TCGA- ETLVRPKPLLLKLLKSVGAQKDTYTMKEVLFYL 19- GQYIMTKRLYDEKQQHIVYCSNDLLGDLFGVP 2624- SFSVKEHRKIYTMIYRNLVVVNQQESSDSGTS 01A- VSENRCHLEGGSDQKDLVQELQEEKPSSSHLV 01R- SRPSTSSRRRAISETEENSDELSGERQRKRHKS 1850- DSISLSFDESLALCVIREICCERSSSSESTGTPSN 01.2 PDLDAGVSEHSGDWLDQDSVSDQFSVEFEVE SLDSEDYSLSEEGQELSDEDDEVYQVTVYQAG ESDTDSFEEDPEISLAESEGVSCHYWSLFDGH AGSGAAVVASRLLQHHITEQLQDIVDILKNSA VLPPTCLGEEPENTPANSRTLTRAASLRGGVG APGSPSTPPTRFFTEKKIPHECLVIGALESAFKE MDLQIERERSSYNISGGCTALIVICLLGKLYVAN AGDSRAIIIRNGEIIPMSSEFTPETERQRLQYLA FMQPHLLGNEFTHLEFPRRVQRKELGKKMLY RDFNMTGWAYKTIEDEDLKFPLIYGEGKKARV MATIGVTRGLGDHDLKVHDSNIYIKPFLSSAPE VRIYDLSKYDHGSDDVLILATDGLWDVLSNEE VAEAITQFLPNCDPDDPHRYTLAAQDLVMRA RGVLKDRGWRISNDRLGSGDDISVYVIPLIHG NKLS G17484. 1 2002 24 156 8428 MDPRNTAMLGLGSDSEGFSRKSPSAISTGTLV 6 4 TCGA- SKREVELEKNTKEEEDLRKRNRERNIEAGKDD 14- GLTDAQQQFSVKETNFSEGNLKLKIGLQAKRT 0787- KKPPKNLENYVCRPAIKTTIKHPRKALKSGKMT 01A- DEKNEHCPSKRDPSKLYKKADDVAAIECQSEE 01R- VIRLHSQGENNPLSKKLSPVHSEMADYINATP 1849- STLLGSRDPDLKDRALLNGGTSVTEKLAQLIAT 01.2 CPPSKSSKTKPKKLGTGTTAGLVSKDLIRKAGV GSVAGIIHKDLIKKPTISTAVGLVTKDPGKKPVF NAAVGLVNKDSVKKLGTGTTAVFINKNLGKKP GTITTVGLLSKDSGKKLGIGIVPGLVHKESGKKL GLGTVVGLVNKDLGKKLGSTVGLVAKDCAKKI VASSAMGLVNKDIGKKLMSCPLAGLISKDAIN LKAEALLPTQEPLKASCSTNINNQESQELSESL KDSATSKTFEKNVVRQNKESILEKFSVRKEIINL EKEMFNEGTCIQQDSFSSSEKGSYETSKHEKQ PPVYCTSPDFKMGGASDVSTAKSPFSAVGES NLPSPSPTVSVNPLTRSPPETSSQLAPNPLLLSS TTELIEEISESVGKNQFTSESTHLNVGHRSVGH SISIECKGIDKEVNDSKTTHIDIPRISSSLGKKPSL TSESSIHTITPSVVNFTSLFSNKPFLKLGAVSAS DKHCQVAESLSTSLQSKPLKKRKGRKPRWTKV VARSTCRSPKGLELERSELFKNVSCSSLSNSNSE PAKFMKNIGPPSFVDHDFLKRRLPKLSKSTAPS LALLADSEKPSHKSFATHKLSSSMCVSSDLLSDI YKPKRGRPKSKEMPQLEGPPKRTLKIPASKVFS LQSKEEQEPPILQPEIEIPSFKQGLSVSPFPKKR GRPKRQMRSPVKMKPPVLSVAPFVATESPSK LESESDNHRSSSDFFESEDQLQDPDDLDDSHR PSVCSMSDLEMEPDKKITKRNNGQLMKTIIRK INKMKTLKRKKLLNQILSSSVESSNKGKVQSKL HNTVSSLAATFGSKLGQQINVSKKGTIYIGKRR GRKPKTVLNGILSGSPTSLAVLEQTAQQAAGS ALGQILPPLLPSSASSSEILPSPICSQSSGTSGGQ SPVSSDAGFVEPSSVPYLHLHSRQGSMIQTLA MKKASKGRRRLSPPTLLPNSPSHLSELTSLKEA TPSPISESHSDETIPSDSGIGTDNNSTSDRAEKF CGQKKRRHSFEHVSLIPPETSTVLSSLKEKHKH KCKRRNHDYLSYDKMKRQKRKRKKKYPQLRN RQDPDFIAELEELISRLSEIRITHRSHHFIPRDLL PTIFRINFNSFYTHPSFPLDPLHYIRKPDLKKKR GRPPKMREAMAEMPFMHSLSFPLSSTGFYPS YGMPYSPSPLTAAPIGLGYYGRYPPTLYPPPPS PSFTTPLPPPSYMHAGHLLLNPAKYHKKKHKL LRQEAFLTTSRTPLLSMSTYPSVPPEMAYGW MVEHKHRHRHKHREHRSSEQPQVSMDTGSS RSVLESLKRYRFGKDAVGERYKHKEKHRCHMS CPHLSPSKSLINREEQWVHREPSESSPLALGLQ TPLQIDCSESSPSLSLGGFTPNSEPASSDEHTNL FTSAIGSCRVSNPNSSGRKKLTDSPGLFSAQDT SLNRLHRKESLPSNERAVQTLAGSQPTSDKPS QRPSESTNCSPTRKRSSSESTSSTVNGVPSRSP RLVASGDDSVDSLLQRMVQNEDQEPMEKSID AVIATASAPPSSSPGRSHSKDRTLGKPDSLLVP AVTSDSCNNSISLLSEKLTSSCSPHHIKRSVVEA MQRQARKMCNYDKILATKKNLDHVNKILKAK KLQRQARTGNNFVKRRPGRPRKCPLQAVVS MQAFQAAQFVNPELNRDEEGAALHLSPDTV TDVIEAVVQSVNLNPEHKKGLKRKGWLLEEQ TRKKQKPLPEEEEQENNKSFNEAPVEIPSPSET PAKPSEPESTLQPVLSLIPREKKPPRPPKKKYQK AGLYSDVYKTTDFSPGAGGFCTTLPPSFLRVD DRATSSTTDSSRAPSSPRPPGSTSHCGISTRCT ERCLCVLPLRTSQVPDVMAPQHDQEKFHDLA YSCLGKSFSMSNQDLYGYSTSSLALGLAWLSW ETKKKNVLHLVGLDSL G17792. 1 326 21 206 8429 MSGGKKKSSFQITSVTTDYEGPGSPGASDPPT 4 2 TCGA- PQPPTGPPPRLPNGEPSPDPGGKGTPRNGSP 28- PPGAPSSRFRVVKLPHGLGEPYRRGRWTCVD 5204- VYERDLEPHSFGGLLEGIRGASGGAGGRSLDS 01A- RLELASLGLGAPTPPSGLSQGPTSWLRPPPTSP 01R- GPQARSFTGGLGQLVVPSKAKAEKPPLSASSP 1850- QQRPPEPETGESAGTSRAATPLPSLRVEAEAG 01.4 GSGARTPPLSRRKAVDMRLRMELGAPEEMG QVPPLDSRPSSPALYFTHDASLVHKSPDPFGA VAAQKFSLAHSMLAISGHLDSDDDSGSGSLV GIDNKIEQAMVFFWRQKIKPTISGHPDSKKHS LKKMEKTLQVVETLRLVELPKEAKPKLGESPEL ADPCVLAKTTEETEVELGQQGQSLLQLPRTAV KSVSTLMVSALQSGWQMCSWKSSVSSASVS SQVRTQSPLKTPEAELLWEVYLVLWAVRKHLR RLYRRQERHRRHHVRCHAAPRPNPAQSLKLD AQSPL BT299 1 20 10 600 8430 MALRRLGAALLLLPLLAAVEGAGQDVGRSCIL VSIAGKNVMLDCGMHMGFNDDRRFPDFSYI TQNGRLTDFLDCVIISHFHLDHCGALPYFSEM VGYDGPIYMTHPTQAICPILLEDYRKIAVDKKG EANFFTSQMIKDCMKKVVAVHLHQTVQVDD ELEIKAYYAGHVLGAAMFQIKVGSESVVYTGD YNMTPDRHLGAAWIDKCRPNLLITESTYATTI RDSKRCRERDFLKKVHETVERGGKVLIPVFALG RAQELCILLETFWERMNLKVPIYFSTGLTEKAN HYYKLFIPWTNQKIRKTFVQRNMFEFKHIKAF DRAFADNPGPMVVFATPGMLHAGQSLQIFR KWAGNEKNMVIMPGYCVQGTVGHKILSGQR KLEMEGRQVLEVKMQVEYMSFSAHADAKGI MQLVGQAEPESVLLVHGEAKKMEFLKQKIEQ ELRVNCYMPANGETVTLPTSPSIPVGISLGLLK REMAQGLLPEAKKPRLLHGTLIMKDSNFRLVS SEQALKELGLAEHQLRFTCRVHLHDTRKEQET ALRVYSHLKSVLKDHCVQHLPDGSVTVESVLL QAAAPSEDPGTKVLLVSWTYQDEELGSFLTSL LKKGLPQAPS G17667. 1 258 50 56 8431 MNQPESANDPEPLCAVCGQAHSLEENHFYSY 4 4 TCGA- PEEVDDDLICHICLQALLDPLDTPCGHTYCTLC 26- LTNFLVEKDFCPMDRKPLVLQHCKKSSILVNKL 5134- LNKLLVTCPFREHCTQVLQRCDLEHHFQTSCK 01A- GASHYGLTKDRKRRSQDGCPDGCASLTATAP 01R- SPEVSAAATISLMTDEPGLDNPAYVSSAEDGQ 1850- PAISPVDSGRSNRTRARPFERSTIRSRSFKKINR 01.2 ALSVLRRTKSGSAVANHADQGRENSENTTAP EVWKHMLL GBM- 1 432 8 609 8432 MWLKVGGLLRGTGGQLGQIVGWPCGALGP 14 2 CUMC3338_L1 GPHRWGPCGGSWAQKFYQDGPGRGLGEED IRRAREARPRKTPRPQLSDRSRERKVPASRISR LANFGGLAVGLGLGVLAEMAKKSMPGGRLQ SEGGSGLDSSPFLSEANAERIVQTLCTVRGAAL KVGQMLSIQDNSFISPQLQHIFERVRQSADF MPRWQMLRVLEEELGRDWQAKVASLEEVPF AAASIGQVHQGLLRDGTEVAVKIQYPGIAQSI QSDVQNLLAVLKMSAALPAGLFAEQSLQALQ QELAWECDYRREAACAQNFRQLLANDPFFRV PAVVKELCTTRVLGMELAGGVPLDQCQGLSQ DLRNQICFQLLTLCLRELFEFRFMQTDPNWAN FLYDASSHQVTLLDFGASREFGTEFTDHYIEVV KAAADGDRDCVLQKSRDLKFLTGFETKGGPR RPERHLPPAPCGAPGPPETCRTEPDGAGTMN KLRQSLRRRKPAYVPEASRPHQWQADEDAVR KGTCSFPVRYLGHVEVEESRGMHVCEDAVKK LKAMGRKSVKSVLWVSADGLRVVDDKTKDLL VDQTIEKVSFCAPDRNLDKAFSYICRDGTTRR WICHCFLALKDSGERLSHAVGCAFAACLERKQ RREKECGVTAAFDASRTSFAREGSFRLSGGGR PAEREAPDKKKAEAAAAPTVAPGPAQPGHVS PTPATTSPGEKGEAGTPVAAGTTAAAIPRRHA PLEQLVRQGSFRGFPALSQKNSPFKRQLSLRL NELPSTLQRRTDFQVKGTVPEMEPPGAGDSD SINALCTQISSSFASAGAPAPGPPPATTGTSA WGEPSVPPAAAFQPGHKRTPSEAERWLEEVS QVAKAQQQQQQQQQQQQQQQQQQQQA ASVAPVPTMPPALQPFPAPVGPFDAAPAQVA VFLPPPHMQPPFVPAYPGLGYPPMPRVPVVG ITPSQMVANAFCSAAQLQPQPATLLGKAGAF PPPAIPSAPGSQARPRPNGAPWPPEPAPAPA PELDPFEAQWAALEGKAIVEKPSNPFSGDLQ KTFEIEL G17815. 1 700 32 192 8433 MASCPDSDNSWVLAGSESLPVETLGPASRM 10 2 TCGA- DPESERALQAPHSPSKTDGKELAGTMDGEGT 19- LFQTESPQSGSILTEETEVKGTLEGDVCGVEPP 5960- GPGDTVVQGDLQETTVVTGLGPDTQDLEGQ 01A- SPPQSLPSTPKAAWIREEGRCSSSDDDTDVD 11R- MEGLRRRRGREAGPPQPMVPLAVENQAGG 1850- EGAGGELGISLNMCLLGALVLLGLGVLLFSGGL 01.4 SESETGPMEEVERQVLPDPEVLEAVGDRQDG LREQLQAPVPPDSVPSLQNMGLLLDKLAKEN QDIRLLQAQLQAQKEELQSLMHQPKGLEEEN AQLRGALQQGEAFQRALESELQQLRARLQGL EADCVRGPDGVCLSGGRGPQGDKAIREQGP REQEPELSFLKQKEQLEAEAQALRQELERQRR LLGSVQQDLERSLQDASRGDPAHAGLAELGH RLAQKLQGLENWGQDPGVSANASKAWHQK SHFQNSREWSGKEKWWDGQRDRKAEHWK HKKEESGRERKKNWGGQEDREPAGRWKEGR PRVEESGSKKEGKRQGPKEPPRKSGSFHSSGE KQKQPRWREGTKDSHDPLPSWAELLRPKYRA PQGCSGVDECARQEGLTFFGTELAPVRQQEL ASLLRTYLARLPWAGQLTKELPLSPAFFGEDGI FRHDRLRFRDFVDALEDSLEEVAVQQTGDDD EVDDFEDFIFSHFFGDKALKKRLGADVCAVLRL SGPLKEQYAQEHGLNFQRLLDTSTYKEAFRKD MIRWGEEKRQADPGFFCRKIVEGISQPIWLVS DTRRVSDIQWFREAYGAVTQIVRVVALEQSR QQRGWVFTPGVDDAESECGLDNFGDFDWVI ENHGVEQRLEEQLENLIEFIRSRL G17662. 1 81 23 977 8434 MEARSMLVPPQASVCFEDVAMAFTQEEWE 3 2 TCGA- QLDLAQRTLYREVTLETWEHIVSLGLFLSKSDV 32- ISQLEQEEDLCRAEQEAPRGKSKEAEIKRINKEL 1970- ANIRSKFKGDKALDGYSKKKYVCKLLFIFLLGH 01A- DIDFGHMEAVNLLSSNKYTEKQIGYLFISVLVN 01R- SNSELIRLINNAIKNDLASRNPTFMCLALHCIA 1850- NVGSREMGEAFAADIPRILVAGDSMDSVKQS 01.2 AALCLLRLYKASPDLVPMGEWTARVVHLLND QHMGVVTAAVSLITCLCKKNPDDFKTCVSLAV SRLSRIVSSASTDLQDYTYYFVPAPWLSVKLLRL LQCYPPPEDAAVKGRLVECLETVLNKAQEPPK SKKVQHSNAKNAILFETISLIIHYDSEPNLLVRA CNQLGQFLQHRETNLRYLALESMCTLASSEFS HEAVKTHIDTVINALKTERDVSVRQRAADLLY AMCDRSNAKQIVSEMLRYLETADYAIREEIVLK VAILAEKYAVDYSWYVDTILNLIRIAGDYVSEE VWYRVLQIVTNRDDVQGYAAKTVFEALQAPA CHENMVKVGGYILGEFGNLIAGDPRSSPPVQF SLLHSKFHLCSVATRALLLSTYIKFINLFPETKATI QGVLRAGSQLRNADVELQQRAVEYLTLSSVA STDVLATVLEEMPPFPERESSILAKLKRKKGPG AGSALDDGRRDPSSNDINGGMEPTPSTVSTP SPSADLLGLRAAPPPAAPPASAGAGNLLVDVF DGPAAQPSLGPTPEEAFLSELEPPAPESPMALL ADPAPAADPGPEDIGPPIPEADELLNKFVCKN NGVLFENQLLQIGVKSEFRQNLGRMYLFYGN KTSVQFQNFSPTVVHPGDLQTHLAVQTKRVA AQVDGGAQVQQVLNIECLRDFLTPPLLSVRFR YGGAPQALTLKLPVTINKFFQPTEMAAQDFF QRWKQLSLPQQEAQKIFKANHPMDAEVTKA KLLGFGSALLDNVDPNPENFVGAGIIQTKALQ VGCLLRLEPNAQAQMYRLTLRTSKEPVSRHLC ELLAQQF NYU_E 1 416 3 148 8435 MASESGKLWGGRFVGAVDPIMEKFNASIAYD 15 2 RHLWEVDVQGSKAYSRGLEKAGLLTKAEMD QILHGLDKVAEEWAQGTFKLNSNDEDIHTAN ERRLKELIGATAGKLHTGRSRNDQVVTDLRLW MRQTCSTLSGLLWELIRTMVDRAEAERDVLF PGYTHLQRAQPIRWSHWILSHAVALTRDSERL LEVRKRINVLPLGSGAIAGNPLGVDRELLRAEL NFGAITLNSMDATSERDFVAEFLFWASLCMT HLSRMAEDLILYCTKEFSFVQLSDAYSTGSSLM PQKKNPDSLELIRSKAGRVFGRCAGLLMTLKG LPSTYNKDLQEDKEAVFEVSDTMSAVLQVAT GVISTLQIHQENMGQALSPDMLATDLAYYLV RKGMPFRQAHEASGKAVFMAETKGVALNQL SLQELQTIRKDANSALLSNYEVFQLLTDLKEQR KESGKNKHSSGQQNLNTITYETLKYISKTPCRH QSPEIVREFLTALKSHKLTKAEKLQLLNHRPVT AVEIQLMVEESEERLTEEQIEALLHTVTSILPAE PEAEQKKNTNSNVAMDEEDPA G17816. 1 982 190 225 8436 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 6 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 28- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 5215- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01A- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 01R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1850- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.4 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTTYQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HTPPLDPQELDILKTVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSTVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQDAFIGFGGNVI RQQVKDNAKWYITDFVELLGELEE G17650. 1 68 18 432 8437 MGETMSKRLKLHLGGEAEMEERAFVNPFPDY 1 3 TCGA- EAAAGALLASGAAEETGCVRPPATTDEPGLPF 28- HQDGKQKENNIRCLTTIGHFGFECLPNQLVSR 2513- SIRQGFTFNILCVGETGIGKSTLIDTLFNTNLKD 01A- NKSSHFYSNVGLQIQTYELQESNVQLKLTVVE 01R- TVGYGDQIDKEASYQPIVDYIDAQFEAYLQEEL 1850- KIKRSLFEYHDSRVHVCLYFISPTGHSLKSLDLLT 01.2 MKNLDSKVNIIPLIAKADTISKNDLQTFKNKIM SELISNGIQIYQLPTDEETAAQANSSVSGLLPFA VVGSTDEVKVGKRMVRGRHYPWGVLQVEN ENHCDFVKLRDMLLCTNMENLKEKTHTQHYE CYRYQKLQKMGFTDVGPNNQPVSFQEIFEAK RQEFYDQCQREEEELKQRFMQRVKEKEATFK EAEKELQDKFEHLKMIQQEEIRKLEEEKKQLEG EIIDFYKMKAASEALQTQLSTDTKKDKHRKK BT308 1 176 2050 2063 8438 MAAPLVLVLVVAVTVRAALFRSSLAEFISERVE 6 16 VVSPLSSWKRVVEGLSLLDLGVSPYSGAVFHE TPLIIYLFHFLIDYAELVFMITDALTAIALYFAIQD FNKVVFKKQKLLLELDQYAPDVAELIRTPMEM RYIPLKVALFYLLNPYTILSCVAKSTCAINNTLIA FFILTTIKDITSAVQSKRRKSK G17656. 1 982 18 172 8439 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 2 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 28- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 2514- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01A- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 02R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1850- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.2 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTTYQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HTPPLDPQELDILKTVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSTVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQCTEAKKHCWYF EGLYPTYYICRSYEDCCGSRCCVRALSIQRLWY FWFLLMMGVLFCCGAGFFIRRRMYPPPLIEEP AFNVSYTRQPPNPGPGAQQPGPPYYTDPGG PGMNPVGNSMAMAFQVPPNSPQGSVACPP PPAYCNTPPPPYEQVVKAK G17639. 1 344 94 262 8440 MAEAPPVSGTFKFNTDAAEFIPQEKKNSGLNC 2 3 TCGA- GTQRRLDSNRIGRRNYSSPPPCHLSRQVPYDE 12- ISAVHQHSYHPSGSKPKSQQTSFQSSPCNKSP 3652- KSHGLQNQPWQKLRNEKHHIRVKKAQSLAE 01A- QTSDTAGLESSTRSESGTDLREHSPSESEKEVV 01R- GADPRGAKPKKATQFVYSYGRGPKVKGKLKC 1849- EWSNRTTPKPEDAGPESTKPVGVFHPDSSEAS 01.2 SRKGVLDGYGARRNEQRRYPQKRPPWEVEG ARPRPGRNPPKQEGHRHTNAGHRNNMGPIP KDDLNERPAKSTCDSENLAVINKSSRRVDQEK CTVRRQDPQVVSPFSRGKQNHVLKNVETHTA DKCSPNYLGSDWYNTWRMEPYNSSCCNKYT TYLPRLPKEARMETAVRGMPLECPPRPERLNA YEREVMVNMLNSLSRNQQLPRITPRCGCVDP LPGRLPFHGYESACSGRHYCLRGMDYYASGA PCTDRRLRPWCREQPTMCTSLRAPARNAVCC YNSPAVILPISEP G17796. 1 193 167 1032 8441 MAAETLLSSLLGLLLLGLLLPASLTGGVGSLNLE 5 7 TCGA- ELSEMRYGIEILPLPVMGGQSQSSDVVIVSSKY 41- KQRYECRLPAGAIHFQREREEETPAYQGPGIP 5651- ELLSPMRDAPCLLKTKDWWTYEFCYGRHIQQ 01A- YHMEDSEIKGEVLYLGYYQSAFDWDDETAKA 01R- SKQHRLKRYHSQTYGNGSKCDLNGRPREAEV 1850- RGCTERFVSSPEEILDVIDEGKSNRHVAVTNM 01.4 NEHSSRSHSIFLINIKQENMETEQKLSGKLYLV DLAGSEKVSKTGAEGAVLDEAKNINKSLSALG NVISALAEGTKSYVPYRDSKMTRILQDSLGGN CRTTMFICCSPSSYNDAETKSTLMFGQRAKTIK NTASVNLELTAEQWKKKYEKEKEKTKAQKETI AKLEAELSRWRNGENVPETERLAGEEAALGA ELCEETPVNDNSSIVVRIAPEERQKYEEEIRRLY KQLDDKDDEINQQSQLIEKLKQQMLDQEELL VSTRGDNEKVQRELSHLQSENDAAKDEVKEV LQALEELAVNYDQKSQEVEEKSQQNQLLVDE LSQKVATMLSLESELQRLQEVSGHQRKRIAEV LNGLMKDLSEFSVIVGNGEIKLPVEISGAIEEEF TVARLYISKIKSEVKSVVKRCRQLENLQVECHR KMEVTGRELSSCQLLISQHEAKIRSLTEYMQSV ELKKRHLEESYDSLSDELAKLQAQETVHEVALK DKEPDTQDADEVKKALELQMESHREAHHRQ LARLRDEINEKQKTIDELKDLNQKLQLELEKLQ ADYEKLKSEEHEKSTKLQELTFLYERHEQSKQD LKGLEETVARELQTLHNLRKLFVQDVTTRVKKS AEMEPEDSGGIHSQKQKISFLENNLEQLTKVH KQLVRDNADLRCELPKLEKRLRATAERVKALE GALKEAKEGAMKDKRRYQQEVDRIKEAVRYK SSGKRGHSAQIAKPVRPGHYPASSPTNPYGTR SPECISYTNSLFQNYQNLYLQATPSSTSDMYFA NSCTSSGATSSGGPLASYQKANMDNGNATDI NDNRSDLPCGYEAEDQAKLFPLHQETAAS G17468. 1 209 176 342 8442 MKLADSVMAGKASDGSIKWQLCYDISARTW 2 5 TCGA- WMDEFHPFIEALLPHVRAFAYTWFNLQARKR 19- KYFKKHEKRMSKEEERAVKDELLSEKPEVKQK 0957- WASRLLAKLRKDIRPEYREDFVLTVTGKKPPCC 02A- VLSNPDQKGKMRRIDCLRQADKVWRLDLVM 11R- VILFKGIPLESTDGERLVKSPQCSNPGLCVQPH 2005- HIGVSVKELDLYLAYFVHAAVISECQRQQLEAV 01.2 SYSSRYALGLFYEAGTKIDVPWAGQYITSNPCI RFVSIDNKKRNIESSEIGPSLVIHTTVPFGVTYLE HSIEDVQELVFQQLENILPGLPQPIATKCQKW RHSQVTNAAANCPGQMTLHHKPFLACGGDG FTQSNFDGCITSALCVLEALKNYI G17790. 1 386 211 319 8443 MMLRGNLKQVRIEKNPARLRALESAVGESEP 6 6 TCGA- AAAAAMALALAGEPAPPAPAPPEDHPDEEM 06- GFTIDIKSFLKPGEKTYTQRCRLFVGNLPTDITE 5856- EDFKRLFERYGEPSEVFINRDRGFGFIRLESRTL 01A- AEIAKAELDGTILKSRPLRIRFATHGAALTVKNL 01R- SPVVSNELLEQAFSQFGPVEKAVVVVDDRGR 1849- ATGKGFVEFAAKPPARKALERCGDGAFLLTTT 01.4 PRPVIVEPMEQFDDEDGLPEKLMQKTQQYHK EREQPPRFAQPGTFEFEYASRWKALDEMEKQ QREQVDRNIREAKEKLEAEMEAARHEHQLML MRQDLMRRQEELRRLEELRNQELQKRKQIQL RHEEEHRRREEEMIRHREQEELRRQQEGFKP NYMENEGIVSPSDLDLVMSEGLGMRYAFIGP LETMHLNAEGMLSYCDRYSEGIKHVLQTFGPI PEFSRATAEKVNQDMCMKVPDDPEHLAARR QWRDECLMRLAKLKSQVQPQ GBM- 1 447 160 327 8444 MKETIQGTGSWGPEPPGPGIPPAYSSPRRERL 8 6 CUMC3338_L1 RWPPPPKPRLKSGGGFGPDPGSGTTVPARRL PVPRPSFDASASEEEEEEEEEEDEDEEEEVAA WRLPPRWSQLGTSQRPRPSRPTHRKTCSQRR RRAMRAFRMLLYSKSTSLTFHWKLWGRHRG RRRGLAHPKNHLSPQQGGATPQVPSPCCRFD SPRGPPPPRLGLLGALMAEDGVRGSPPVPSG PPMEEDGLRWTPKSPLDPDSGLLSCTLPNGF GGQSGPEGERSLAPPDASILISNVCSIGDHVA QELFQGSDLGMAEEAERPGEKAGQHSPLREE HVTCVQSILDEFLQTYGSLIPLSTDEVVEKLEDI FQQEFSTPSRKGLVLQLIQSYQRMPGNAMVR GFRVAYKRHVLTMDDLGTLYGQNWLNDQV MNMYGDLVMDTVPEKVHFFNSFFYDKLRTK GYDGVKRWTKNTRHYVGSAAAFAGTPEHGQ FQGSPGGAYGTAQPPPHYGPTQPAYSPSQQL RAPSAFPAVQYLSQPQPQPYAVHGHFQPTQT GFLQPGGALSLQKQMEHANQQTGFSDSSSLR PMHPQALHPAPGLLASPQLPVQMQPAGKSG FAATSQPGPRLPFIQHSQNPRFYHK G17790. 1 37 228 497 8445 MVNLAAMVWRRLLRKRWVLALVFGLSLVYFL 1 9 TCGA- SSTFKQDLDAGVSEHSGDWLDQDSVSDQFSV 06- EFEVESLDSEDYSLSEEGQELSDEDDEVYQVTV 5856- YQAGESDTDSFEEDPEISLADYWKCTSCNEM 01A- NPPLPSHCNRCWALRENWLPEDKGKDKGEIS 01R- EKAKLENSTQAEEGFDVPDCKKTIVNDSRESC 1849- VEENDDKITQASQSQESEDYSQPSTSSSIIYSSQ 01.4 EDVKEFEREETQDKEESVESSLPLNAIEPCVICQ GRPKNGCIVHGKTGHLMACFTCAKKLKKRNK PCPVCRQPIQMIVLTYFP G17802. 1 344 240 432 8446 MDAPRASAAKPPTGRKMKARAPPPPGKAAT 7 7 TCGA- LHVHSDQKPPHDGALGSQQNLVRMKEALRA 28- STMDVTVVLPSGLEKRSVLNGSHAMMDLLVE 5208- LCLQNHLNPSHHALEIRSSETQQPLSFKPNTLI 01A- GTLNVHTVFLKEKVPEEKVKPGPPKVPEKSVRL 01R- VVNYLRTQKAVVRVSPEVPLQNILPVICAKCEV 1850- SPEHVVLLRDNIAGEELELSKSLNELGIKELYA 01.4 WDNRRETFRKSSLGNDETDKEKKKFLGFFKVN KRSNSKAEQLVLSGADSDEDTSRAAPGRGLN GCLTTPNSPSMHSRSLTLGPSLSLGSISGVSVK SEMKKRRAPPPPGSGPPVQDKASEKGLLPFA VVGSTDEVKVGKRMVRGRHYPWGVLQVEN ENHCDFVKLRDMLLCTNMENLKEKTHTQHYE CYRYQKLQKMGFTDVGPNNQPVSFQEIFEAK RQEFYDQCQREEEELKQRFMQRVKEKEATFK EAEKELQDKFEHLKMIQQEEIRKLEEEKKQLEG EIIDFYKMKAASEALQTQLSTDTKKDKHRKK G17210. 1 149 141 188 8447 MKLALLLPWACCCLCGSALATGFLYPFSAAAL 4 4 TCGA- QQHGYPEPGAGSPGSGYASRRHWCHHTVTR 12- TVSCQVQNGSETVVQRVYQSCRWPGPCANL 0616- VSYRTLIRPTYRVSYRTVTVLEWRCCPGFTGSN 01A- CDEECMNCTRLSDMSERLTTLEAKIICMGAKE 01R- NGLPLEYQEKLKAIEPNDYTGKVSEEIEDIIKKG 1849- ETQTL 01.2 NYU_B 1 89 380 1104 8448 MAAETQTLNFGPEWLRALSSGGSITSPPLSPA 4 10 LPKYKLADYRYGREEMLALFLKDNKIPSDLLDK EFLPILQEEPLPPLALVPFTEEEQLKEILECSHLLT VIKMEEAGDEIVSNAISYALYKAFSTSEQDKDN WNGQLKLLLEWNQLDLANDEIFTNDRRWES ADLQEVMFTALIKDRPKFVRLFLENGLNLRKFL THDVLTELFSNHFSTLVYRNLQIAKNSYNDALL TFVWKLVANFRRGFRKEDRNGRDEMDIELHD VSPITRHPLQALFIWAILQNKKELSKVIWEQTR GCTLAALGASKLLKTLAKVKNDINAAGESEELA NEYETRAVELFTECYSSDEDLAEQLLVYSCEAW GGSNCLELAVEATDQHFIAQPGVQNFLSKQW YGEISRDTKNWKIILCLFIIPLVGCGFVSFRKKPV DKHKKLLWYYVAFFTSPFVVFSWNVVFYIAFLL LFAYVLLMDFHSVPHPPELVLYSLVFVLFCDEV RQWYVNGVNYFTDLWNVMDTLGLFYFIAGI VFRLHSSNKSSLYSGRVIFCLDYIIFTLRLIHIFTV SRNLGPKIIMLQRMLIDVFFFLFLFAVWMVAF GVARQGILRQNEQRWRWIFRSVIYEPYLAMF GQVPSDVDGTTYDFAHCTFTGNESKPLCVELD EHNLPRFPEWITIPLVCIYMLSTNILLVNLLVA MFGYTVGTVQENNDQVWKFQRYFLVQEYCS RLNIPFPFIVFAYFYMVVKKCFKCCCKEKNMES SVCCFKNEDNETLAWEGVMKENYLVKINTKA NDTSEEMRHRFRQLDTKLNDLKGLLKEIANKI K G17469. 1 982 373 432 8449 MRPSGTAGAALLALLAALCPASRALEEKKVCQ 24 10 TCGA- GTSNKLTQLGTFEDHFLSLQRMFNNCEVVLG 06- NLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVE 2557- RIPLENLQIIRGNMYYENSYALAVLSNYDANKT 01A- GLKELPMRNLQEILHGAVRFSNNPALCNVESI 01R- QWRDIVSSDFLSNMSMDFQNHLGSCQKCDP 1849- SCPNGSCWGAGEENCQKLTKIICAQQCSGRC 01.2 RGKSPSDCCHNQCAAGCTGPRESDCLVCRKF RDEATCKDTCPPLMLYNPTEYQMDVNPEGKY SFGATCVKKCPRNYVVTDHGSCVRACGADSY EMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDS LSINATNIKHFKNCTSISGDLHILPVAFRGDSFT HTPPLDPQELDILKTVKEITGFLLIQAWPENRT DLHAFENLEIIRGRTKQHGQFSLAVVSLNITSL GLRSLKEISDGDVIISGNKNLCYANTINWKKLF GTSGQKTKIISNRGENSCKATGQVCHALCSPE GCWGPEPRDCVSCRNVSRGRECVDKCNLLEG EPREFVENSECIQCHPECLPQAMNITCTGRGP DNCIQCAHYIDGPHCVKTCPAGVMGENNTLV WKYADAGHVCHLCHPNCTYGCTGPGLEGCP TNGPKIPSIATGMVGALLLLLVVALGIGLFMRR RHIVRKRTLRRLLQERELVEPLTPSGEAPNQAL LRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK VKIPVAIKELREATSPKANKEILDEAYVMASVD NPHVCRLLGICLTSTVQLITQLMPFGCLLDYVR EHKDNIGSQYLLNWCVQIAKGMNYLEDRRLV HRDLAARNVLVKTPQHVKITDFGLAKLLGAEE KEYHAEGGKVPIKWMALESILHRIYTHQSDV WSYGVTVWELMTFGSKPYDGIPASEISSILEK GERLPQPPICTIDVYMIMVKCWMIDADSRPK FRELIIEFSKMARDPQRYLVIQLQDKFEHLKMI QQEEIRKLEEEKKQLEGEIIDFYKMKAASEALQ TQLSTDTKKDKHRKK G17480. 1 471 331 737 8450 MITSAAGIISLLDEDEPQLKEFALHKLNAVVND 12 6 TCGA- FWAEISESVDKIEVLYEDEGFRSRQFAALVASK 27- VFYHLGAFEESLNYALGAGDLFNVNDNSEYVE 1830- TIIAKCIDHYTKQCVENADLPEGEKKPIDQRLE 01A- GIVNKMFQRCLDDHKYKQAIGIALETRRLDVF 01R- EKTILESNDVPGMLAYSLKLCMSLMQNKQFR 1850- NKVLRVLVKIYMNLEKPDFINVCQCLIFLDDPQ 01.2 AVSDILEKLVKEDNLLMAYQICFDLYESASQQF LSSVIQNLRTVGTPIASVPGSTNTGTVPGSEKD SDSMETEEKTSSAFVGKTPEASPEPKDQTLKM IKILSGEMAIELHLQFLIRNNNTDLMILKNTKD AVRNSVCHTATVIANSFMHCGTTSDQFLRDN LEWLARATNWAKFTATASLGVIHKGHEKEAL QLMATYLPKDTSPGSAYQEGGGLYALGLIHA NHGGDIIDYLLNQLKNASNDATFSCTCEEQYV GTFCEEYDACQRKPCQNNASCIDANEKQDGS NFTCVCLPGYTGELCQSKIDYCILDPCRNGATC ISSLSGFTCQCPEGYFGSACEEKVDPCASSPCQ NNGTCYVDGVHFTCNCSPGFTGPTCAQLIDF CALSPCAHGTCRSVGTSYKCLCDPGYHGLYCE EEYNECLSAPCLNAATCRDLVNGYECVCLAEY KGTHCELYKDPCANVSCLNGATCDSDGLNGT CICAPGFTGEECDIDINECDSNPCHHGGSCLD QPNGYNCHCPHGWVGANCEIHLQWKSGH MAESLTNMPRHSLYIIIGALCVAFILMLIILIVGI CRISRIEYQGSSRPAYEEFYNCRSIDSEFSNAIAS IRHARFGKKSRPAMYDVSPIAYEDYSPDDKPL VTLIKTKDL G17634. 1 62 2 132 8451 MAEGAQPHQPPQLGPGAAARGMKRESELEL 1 2 TCGA- PVPGAGGDGADPGLSKRPRTEEAAADGGGG 19- MQGELEVKNMDMKPGSTLKITGSIADGTDGF 2625- VINLGQGTDKLNLHFNPRFSESTIVCNSLDGSN 01A- WGQEQREDHLCFSPGSEVKFTVTFESDKFKVK 01R- LPDGHELTFPNRLGHSHLSYLSVRGGFNMSSF 1850- KLKE 01.2 G17654. 1 151 467 758 8452 MDRPGFVAALVAGGVAGVSVDLILFPLDTIKT 6 13 TCGA- RLQSPQGFSKAGGFHGIYAGVPSAAIGSFPNA 41- AAFFITYEYVKWFLHADSSSYLTPMKHMLAAS 4097- AGEVVACLIRVPSEVVKQRAQVSASTRTFQIFS 01A- NILYEEGIQGLYRGYKSTVLREIEEVRDAMENE 01R- MRTQLRRQAAAHTDHLRDVLRVQEQELKSEF 1850- EQNLSEKLSEQELQFRRLSQEQVDNFTLDINT 01.2 AYARLRGIEQAVQSHAVAEEEARKAHQLWLS VEALKYSMKTSSAETPTIPLGSAVEAIKANCSD NEFTQALTAAIPPESLTRGVYSEETLRARFYAV QKLARRVAMIDETRNSLYQYFLSYLQSLLLFPP QQLKPPPELCPEDINTFKLLSYASYCIEHGDLEL AAKFVNQLKGESRRVAQDWLKEARMTLETK QIVEILTAYASAVGIGTTQVQPE G17485. 1 25 118 369 8453 MGVPKFYRWISERYPCLSEVVKEHQVICNSFTI 1 6 TCGA- CNAEMQEVGVGLYPSISLLNHSCDPNCSIVFN 14- GPHLLLRAVRDIEVGEELTICYLDMLMTSEERR 1402- KQLRDQYCFECDCFRCQTQDKDADMLTGDE 02A- QVWKEVQESLKKIEELKAHWKWEQVLAMCQ 01R- AIISSNSERLPDINIYQLKVLDCAMDACINLGLL 2005- EEALFYGTRTMEPYRIFFPGSHPVRGVQVMK 01.2 VGKLQLHQGMFPQAMKNLRLAFDIMRVTHG REHSLIEDLILLLEECDANIRAS G17498. 1 338 85 225 8454 MAAAGARLSPGPGSGLRGRPRLCFHPGPPPL 3 3 TCGA- LPLLLLFLLLLPPPPLLAGATAAASREPDSPCRLK 02- TVTVSTLPALRESDIGWSGARAGAGAGTGAG 2483- AAAAAASPGSPGSAGTAAESRLLLFVRNELPG 01A- RIAVQDDLDNTELPFFTLEMSGTAADISLVHW 01R- RQQWLENGTLYFHVSMSSSGQLAQATAPTL 1849- QEPSEIVEEQMHILHISVMGGLIALLLLLLVFTV 01.2 ALYAQRRWQKRRRIPQKSASTEATHEIHYIPS VLLGPQARESFRSSRLQTHNSVIGVPIRETPILD DYDCEEDEEPPRRANHVSREDEFGSQVTHTL DSLGHPGEEKVDFEKKDPSLPNVQVTRLTLLSE QAPGPVVMDLTGDLAVLKDQVFVLKEGVDY RVKISFKVHREIVSGLKCLHHTYRRGLRVDKTV YMVGSYGPSAQEYEFVTPVEEAPRGALVRGP YLVVSLFTDDDRTHHLSWEWGLCICQDWKD G17799. 1 613 256 282 8455 MLRLQMTDGHISCTAVEFSYMSKISLNTPPGT 12 10 TCGA- KVKLSGIVDIKNGFLLLNDSNTTVLGGEVEHLIE 06- KWELQRSLSKHNRSNIGTEGGPPPFVPFGQK 1804- CVSHVQVDSRELDRRKTLQVTMPVKPTNDN 01A- DEFEKQRTAAIAEVAKSKETKTFGGGGGGARS 01R- NLNMNAAGNRNREVLQKEKSTKSEGKHEGV 1849- YRELVDEKALKHITEMGFSKEASRQALMDNG 01.4 NNLEAALNVLLTSNKQKPVMGPPLRGRGKGR GRIRSEDEEDLGNARPSAPSTLFDFLESKMGTL NVEEPKSQPQQLHQGQYRSSNTEQNGVKDN NHLRHPPRNDTRQPRNEKPPRFQRDSQNSKS VLEGSGLPRNRGSERPSTSSVSEVWAEDRIKC DRPYSRYDRTKDTSYPLGSQHSDGAFKKRDNS MQSRSGKGPSFAEAKENPLPQGSVDYNNQK RGKRESQTSIPDYFYDRKSQTINNEAFSGIKIEK HFNVNTDYQNPVRSNSFIGVPNGEVEMPLKG RRIGPIKPAGPVTAVPCDDKIFYNSGPKRRSGP IKPEKILESSIPMEYAKMWKPGDECFALYWED NKFYRAEVEALHSSGMTAVVKFIDYGNYEEVL LSNIKPIQTEAWGYDHSYYFIATFITDHIRHHA KYLNA G17660. 1 555 34 526 8456 MADPGMMSLFGEDGNIFSEGLEGLGECGYPE 2 2 TCGA- NPVNPMGQQMPIDQGFASLQPSLHHPSTNQ 06- NQTKLTHFDHYNQYEQQKMHLMDQPNRM 5414- MSNTPGNGLASPHSQYHTPPVPQVPHGGSG 01A- GGQMGVYPGMQNERHGQSFVDSSSMWGP 01R- RAVQVPDQIRAPYQQQQPQPQPPQPAPSGP 1849- PAQGHPQHMQQMGSYMARGDFSMQQHG 01.2 QPQQRMSQFSQGQEGLNQGNPFIATSGPGH LSHVPQQSPSMAPSLRHSVQQFHHHPSTALH GESVAHSPRFSPNPPQQGAVRPQTLNFSSRS QTVPSPTINNSGQYSRYPYSNLNQGLVNNTG MNQNLGLTNNTPMNQSVPRYPNAVGFPSNS GQGLMHQQPIHPSGSLNQMNTQTMHPSQP QGTYASPPPMSPMKAMSNPAGTPPPQVRP GSAGIPMEVGSYPNMPHPQPSHQPPGAMGI GQRNMGPRNMQQSRPFIGMSSAPRELTGH MRPNGCPGVGLGDPQAIQERLIPGQQHPGQ QPSFQQLPTCPPLQPHPGLHHQSSPPHPHHQ PWAQLHPSPQNTPQKVPVHQFDGENMYMS MTEPSQDYVPASQSYPGPSLESEDFNIPPITPP SLPDHSLVHLNEVESGYHSLCHPMNHNGLLPF HPQNMDLPEITVSNMLGQDGTLLSNSISVMP DIRNPEGTQYSSHPQMAAMRPRGQPADIRQ QPGMMPHGQLTTINQSQLSAQLGLNMGGS NVPHNSPSPPGSKSATPSPSSSVHEDEGDDTS KINGGEKRPASDMGKKPKTPKKKKKKDPNEP QKPVSAYALFFRDTQAAIKGQNPNATFGEVSK IVASMWDGLGEEQKQVYKKKTEAAKKEYLKQ LAAYRASLVSKSYSEPVDVKTSQPPQLINSKPS VFHGPSQAHSALYLSSHYHQQPGMNPHLTA MHPSLPRNIAPKPNNQMPVTVSIANMAVSP PPPLQISPPLHQHLNMQQHQPLTMQQPLGN QLPMQVQSALHSPTMQQGFTLQPDYQTIINP TSTAAQVVTQAMEYVRSGCRNPPPQPVDW NNDYCSSGGMQRDKALYLT GBM- 1 163 627 1210 8457 MASASYHISNLLEKMTSSDKDFRFMATNDLM 4 16 CUMC3296_L1 TELQKDSIKLDDDSERKVVKMILKLLEDKNGEV QNLAVKCLGPLVSKVKEYQVETIVDTLCTNML SDKEQLRDISSIGLKTVIGELPPASSGSALAANV CKKITGRLTSAIAKQEDVSVQLEALDIMADML SRCTGPGLEGCPTNGPKIPSIATGMVGALLLLL VVALGIGLFMRRRHIVRKRTLRRLLQERELVEP LTPSGEAPNQALLRILKETEFKKIKVLGSGAFGT WKGLWIPEGEKVKIPVAIKELREATSPKANKEI LDEAYVMASVDNPHVCRLLGICLTSIVQLITQL MPFGCLLDYVREHKDNIGSQYLLNWCVQIAK GMNYLEDRRLVHRDLAARNVLVKTPQHVKIT DFGLAKLLGAEEKEYHAEGGKVPIKWMALESI LHRIYTHQSDVWSYGVTVWELMTFGSKPYD GIPASEISSILEKGERLPQPPICTIDVYMIMVKC WMIDADSRPKFRELIIEFSKMARDPQRYLVIQ GDERMHLPSPTDSNFYRALMDEEDMDDVVD ADEYLIPQQGFFSSPSTSRTPLLSSLSATSNNST VACIDRNGLQSCPIKEDSFLQRYSSDPTGALTE DSIDDTFLPVPEYINQSVPKRPAGSVQNPVYH NQPLNPAPSRDPHYQDPHSTAVGNPEYLNTV QPTCVNSTFDSPAHWAQKGSHQISLDNPDY QQDFFPKEAKPNGIFKGSTAENAEYLRVAPQS SEFIGA G17505. 1 40 525 1132 8458 MNNLNDPPNWNIRPNSRADGGDGSRWNY 2 3 TCGA- ALLVPMLGLAAFRVGCVPAAEHRLREEILAKFL 06- HWLMSVYVVELLRSFFYVTETTFQKNRLFFYR 2564- KSVWSKLQSIGIRQHLKRVQLRELSEAEVRQH 01A- REARPALLTSRLRFIPKPDGLRPIVNMDYVVGA 01R- RTFRREKRAERLTSRVKALFSVLNYERARRPGL 1849- LGASVLGLDDIHRAWRTFVLRVRAQDPPPELY 01.2 FVKVDVTGAYDTIPQDRLTEVIASIIKPQNTYC VRRYAVVQKAAHGHVRKAFKSHVSTLTDLQP YMRQFVAHLQETSPLRDAVVIEQSSSLNEASS GLFDVFLRFMCHHAVRIRGKSYVQCQGIPQG SILSTLLCSLCYGDMENKLFAGIRRDGLLLRLVD DFLLVTPHLTHAKTFLRTLVRGVPEYGCVVNLR KTVVNFPVEDEALGGTAFVQMPAHGLFPWC GLLLDTRTLEVQSDYSSYARTSIRASLTFNRGFK AGRNMRRKLFGVLRLKCHSLFLDLQVNSLQIV CTNIYKILLLQAYRFHACVLQLPFHQQVWKNP TFFLRVISDTASLCYSILKAKNAGMSLGAKGAA GPLPSEAVQWLCHQAFLLKLTRHRVTYVPLLG SLRTAQTQLSRKLPGTTLTALEAAANPALPSDF KTILD G17798. 1 280 15 1673 8459 MLGTGPAAATTAATTSSNVSVLQQFASGLKS 6 2 TCGA- RNEETRAKAAKELQHYVTMELREMSQEESTR 32- FYDQLNHHIFELVSSSDANERKGGILAIASLIGV 5222- EGGNATRIGRFANYLRNLLPSNDPVVMEMAS 01A- KAIGRLAMAGDTFTAEYVEFEVKRALEWLGA 01R- DRNEGRRHAAVLVLRELAISVPTFFFQQVQPF 1850- FDNIFVAVWDPKQAIREGAVAALRACLILTTQ 01.4 REPKEMQKPQWYRHTFEEAEKGFDETLAKEK GMNRDDRIHGALLILNELVRISSMEGESVSQS VFCGTSTYCVLNTVPPIEDDHGNSNSSHVKIFL PKKLLECLPKCSSLPKERHRWNTNEEIAAYLITF EKHEEWLTTSPKTRPQNGSMILYNRKKVKYRK DGYCWKKRKDGKTTREDHMKLKVQGVECLY GCYVHSSIIPTFHRRCYWLLQNPDIVLVHYLNV PAIEDCGKPCGPILCSINTDKKEWAKWTKEELI GQLKPMFHGIKWTCSNGNSSSGFSVEQLVQ QILDSHQTKPQPRTHNCLCTGSLGAGGSVHH KCNSAKHRIISPKVEPRTGGYGSHSEVQHNDV SEGKHEHSHSKGSSREKRNGKVAKPVLLHQSS TEVSSTNQVEVPDTTQSSPVSISSGLNSDPDM VDSPVVTGVSGMAVASVMGSLSQSATVFMS EVTNEAVYTMSPTAGPNHHLLSPDASQGLVL AVSSDGHKFAFPTTGSSESLSMLPTNVSEELVL STTLDGGRKIPETTMNFDPDCFLNNPKQGQT YGGGGLKAEMVSSNIRHSPPGERSFSFTTVLT KEIKTEDTSFEQQMAKEAYSSSAAAVAASSLTL TAGSSLLPSGGGLSPSTTLEQMDFSAIDSNKDY TSSFSQTGHSPHIHQTPSPSFFLQDASKPLPVE QNTHSSLSDSGGTFVMPTVKTEASSQTSSCSG HVETRIESTSSLHLMQFQANFQAMTAEGEVT METSQAAEGSEVLLKSGELQACSSEHYLQPET NGVIRSAGGVPILPGNVVQGLYPVAQPSLGN ASNMELSLDHFDISFSNQFSDLINDFISVEGGS STIYGHQLVSGDSTALSQSEDGARAPFTQAE MCLPCCSPQQGSLQLSSSEGGASTMAYMHV AEVVSAASAQGTLGMLQQSGRVFMVTDYSP EWSYPEGGVKVLITGPWQEASNNYSCLFDQIS VPASLIQPGVLRCYCPAHDTGLVTLQVAFNNQ IISNSVVFEYKARALPTLPSSQHDWLSLDDNQF RMSILERLEQMERRMAEMTGSQQHKQASG GGSSGGGSGSGNGGSQAQCASGTGALGSCF ESRVVVVCEKMMSRACWAKSKHLIHSKTFRG MTLLHLAAAQGYATLIQTLIKWRTKHADSIDL ELEVDPLNVDHFSCTPLMWACALGHLEAAVV LYKWDRRAISIPDSLGRLPLGIARSRGHVKLAE CLEHLQRDEQAQLGQNPRIHCPASEEPSTES WMAQWHSEAISSPEIPKGVTVIASTNPELRRP RSEPSNYYSSESHKDYPAPKKHKLNPEYFQTR QEKLLPTALSLEEPNIRKQSPSSKQSVPETLSPS EGVRDFSRELSPPTPETAAFQASGSQPVGKW NSKDLYIGVSTVQVTGNPKGTSVGKEAAPSQ VRPREPMSVLMMANREVVNTELGSYRDSAE NEECGQPMDDIQVNMMTLAEHIIEATPDRIK QENFVPMESSGLERTDPATISSTMSWLASYLA DADCLPSAAQIRSAYNEPLTPSSNTSLSPVGSP VSEIAFEKPNLPSAADWSEFLSASTSEKVENEF AQLTLSDHEQRELYEAARLVQTAFRKYKGRPL REQQEVAAAVIQRCYRKYKQYALYKKMTQAA ILIQSKFRSYYEQKKFQQSRRAAVLIQKYYRSYK KCGKRRQARRTAVIVQQKLRSSLLTKKQDQA ARKIMRFLRRCRHSPLVDHRLYKRSERIEKGQ GT GBM- 1 57 358 372 8460 MARGYGATVSLVLLGLGLALAVIVLAVVLSRH 1 10 CUMC3297_L1 QAPCGPQAFAHAAVAADSKVCSDIGRQETAY LLVYMKMEC GBM- 1 169 341 484 8461 MFVYVLTPGEQSGRRLPGQTWLMFSCFCFSL 4 9 CUMC3342_L1 QDNSFSSTTVTECDEDPVSLHEDQTDCSSLRD ENNKENYPDAGALVEEHAPPSWEPQQQNVE ATVLVDSVLRPSMGNFKSRKPKSIFKAESGRS HGESQETEHVVSSQSECQVRAGTPAHESPQN NAFKCQETVRLQPRSRKDSLESDSSTAIIPHELI RTRQLESVHLKFNQESGALIPLCLRGRLLHGRH FTYKSITGDMAITFVSTGVEGAFATEEHPYAA HGPWLQILLTEEFVEKMLEDLEDLTSPEEFKLP KEYSWPEKKLKVSILPDVVFDSPLH G17500. 1 2661 303 468 8462 MHSAGTPGLSSRRTGNSTSFQPGPPPPPRLLL 16 7 TCGA- LLLLLLSLVSRVPAQPAAFGRALLSPGLAGAAG 27- VPAEEAIVLANRGLRVPFGREVWLDPLHDLVL 1831- QVQPGDRCAVSVLDNDALAQRPGRLSPKRFP 01A- CDFGPGEVRYSHLGARSPSRDRVRLQLRYDAP 01R- GGAVVLPLVLEVEVVFTQLEVVTRNLPLVVEEL 1850- LGTSNALDARSLEFAFQPETEECRVGILSGLGA 01.2 LPRYGELLHYPQVPGGAREGGAPETLLMDCK AFQELGVRYRHTAASRSPNRDWIPMVVELRS RGAPVGSPALKREHFQVLVRIRGGAENTAPKP SFVAMMMMEVDQFVLTALTPDMLAAEDAE SPSDLLIFNLTSPFQPGQGYLVSTDDRSLPLSSF TQRDLRLLKIAYQPPSEDSDQERLFELELEVVD LEGAASDPFAFMVVVKPMNTMAPVVTRNTG LILYEGQSRPLTGPAGSGPQNLVISDEDDLEAV RLEVVAGLRHGHLVILGASSGSSAPKSFTVAEL AAGQVVYQHDDRDGSLSDNLVLRMVDGGG RHQVQFLFPITLVPVDDQPPVLNANTGLTLAE GETVPILPLSLSATDMDSDDSLLLFVLESPFLTT GHLLLRQTHPPHEKQELLRGLWRKEGAFYERT VTEWQQQDITEGRLFYRHSGPHSPGPVTDQF TFRVQDNHDPPNQSGLQRFVIRIHPVDRLPPE LGSGCPLRMVVQESQLTPLRKKWLRYTDLDT DDRELRYTVTQSPTDTDENHLPAPLGTLVLTD NPSVVVTHFTQAQINHHKIAYRPPGQELGVA TRVAQFQFQVEDRAGNVAPGTFTLYLHPVDN QPPEILNTGFTIQEKGHHILSETELHVNDVDTD VAHISFTLTQAPKHGHMRVSGQILHVGGLFHL EDIKQGRVSYAHNGDKSLTDSCSLEVSDRHHV VPITLRVNVRPVDDEVPILSHPTGTLESYLDVLE NGATEITANVIKGTNEETDDLMLTFLLEDPPLY GEILVNGIPAEQFTQRDILEGSVVYTHTSGEIGL LPKADSFNLSLSDMSQEWRIGGNTIQGVTIW VTILPVDSQAPEIFVGEQLIVMEGDKSVITSVHI SAEDVDSLNDDILCTIVIQPTSGYVENISPAPGS EKSRAGIAISAFNLKDLRQGHINYVQSVHKGV EPVEDRFVFRCSDGINFSERQFFPIVIIPTNDEQ PEMFMREFMVMEGMSLVIDTPILNAADADV PLDDLTFTITQFPTHGHIMNQLINGTVLVESFT LDQIIESSSIIYEHDDSETQEDSFVIKLTDGKHSV EKTVLIIVIPVDDETPRMTINNGLEIEIGDTKIIN NKILMATDLDSEDKSLVYIIRYGPGHGLLQRRK PTGAFENITLGMNFTQDEVDRNLIQYVHLGQ EGIRDLIKFDVTDGINPLIDRYFYVSIGSIDIVFP DVISKGVSLKEGGKVTLTTDLLSTSDLNSPDEN LVFTITRAPMRGHLECTDQPGVSITSFTQLQLA GNKIYYIHTADDEVKMDSFEFQVTDGRNPVF RTFRISISDVDNKKPVVTIHKLVVSESENKLITPF ELTVEDRDTPDKLLKFTITQVPIHGHLLFNNTR PVMVFTKQDLNENLISYKHDGTESSEDSFSFT VTDGTHTDFYVFPDTVFETRRPQVMKIQVLA VDNSVPQIAVNKGASTLRTLATGHLGFMITSKI LKVEDRDSLHISLRFIVTEAPQHGYLLNLDKGN HSITQFTQADIDDMKICYVLREGANATSDMFY FAVEDGGGNKLTYQNFRLNWAWISFEKEYYL VNEDSKFLDVVLKRRGYLGETSFISIGTRDRTA EKDKDFKGKAQKQVQFNPGQTRATWRVRILS DGEHEQSETFQVVLSEPVLAALEFPTVAIVEIV DPGDEPTVFIPQSKYSVEEDVGELFIPIRRSGD VSQELMVVCYTQQGTATGIVPTSVLSYSDYIS RPEDHTSVVRFDKDEREKLCRIVIIDDSLYEEEE TFHVLLSMPMGGRIGSEFPGAQVTIVPDKDD EPIFYFGDVEYSVDESAGYVEVQVWRTGTDLS KSSSVTVRSRKTDPPSADAGTDYVGISRNLDF APGVNMQPVRVVILDDLGQPALEGIEKFELVL RMPMNAALGEPSKATVSINDSVSDLPKMQFK ERIYTGSESDGQIVTMIHRTGDVQYRSSVRCY TRQGSAQVMMDFEERPNTDTSIITFLPGETEK PCILELMDDVLYEEVEELRLVLGTPQSNSPFGA AVGEQNETLIRIRDDADKTVIKFGETKFSVTEP KEPGESVVIRIPVIRQGDTSKVSIVRVHTKDGS ATSGEDYHPVSEEIEFKEGETQHVVEIEVTFDG VREMREAFTVHLKPDENMIAEMQLTKAIVYIE EMSSMADVTFPSVPQIVSLLMYDDTSKAKES AEPMSGYPVICITACNPKYSDYDKTGSICASEN INDTLTRYRWLISAPAGPDGVTSPMREVDFDT FFTSSKMVTLDSIYFQPGSRVQCAARAVNTNG DEGLELMSPIVTISREEGLCQPRVPGVVGAEPF SAKLRYTGPEDADYTNLIKLTVTMPHIDGMLP VISTRELSNFELTLSPDGTRVGNHKCSNLLDYT EVKTHYGFLTDATKNPEIIGETYPYQYSLSIRGS TTLRFYRNLNLEACLWEFVSYYDMSELLADCG GTIGTDGQVDVKLDPKDLRIDTFRAKGAGGQ HVNKTDSAVRLVHIPTGLVVECQQERSQIKNK EIAFRVLRARLYQQIIEKDKRQQQSARKLQVG TRAQSERIRTYNFTQDRVSDHRIAYEVRDIKA QSHSTGGSRDPAHSTFLSLDSVRSPGILIMTSS VRNFYVVGRAWIS G17212. 1 304 415 655 8463 MAIDRRREAAGGGPGRQPAPAEENGSLPPG 3 4 TCGA- DAAASAPLGGRAGPGGGAEIQPLPPLHPGGG 06- PHPSCCSAAAAPSLLLLDYDGSVLPFLGGLGG 0129- GYQKTLVLLTWIPALFIGFSQFSDSFLLDQPNF 01A- WCRGAGKGTELAGVTTTGRGGDMGNWTSL 01R- PTTPFATAPWEAAGNRSNSSGADGGDTPPLP 1849- SPPDKGDNASNCDCRAWDYGIRAGLVQNVV 01.2 SKWDLVCDNAWKVHIAKFSLLVGLIFGYLITG CIADWVGRRPVLLFSIIFILIFGLTVALSVNVTM FSTLRFFEGFCLAGIILTLYALRIDILKLVAAQVG SQWKDIYQFLCNASEREVAAFSNGYTADHER AYAALQHWTIRGPEASLAQLISALRQHRRND VVEKIRGLMEDTTQLETDKLALPMSPSPLSPSP IPSPNAKLENSALLTVEPSPQDKNKGFFVDESE PLLRCDSTSSGSSALSRNGSFITKEKKDTVLRQ VRLDPCDLQPIFDDMLHFLNPEELRVIEEIPQA EDKLDRLFEIIGVKSQEASQTLLDSVYSHLPDLL GBM- 1 4 641 1066 8464 MENTDRKVSSLHTSRVQRQMVVSVHDLPEKS 2 16 CUMC3322_L1 FVPLLDSKYVLCVWDIWQPSGPQKVLICESQV TCCCLSPLKAFLLFAGTAHGSVVVWDLREDSR LHYSVTLSDGFWTFRTATFSTDGILTSVNHRSP LQAVEPISTSVHKKQSFVLSPFSTQEEMSGLSF HIASLDESGVLNVWVVVELPKADIAGSISDLGL MPGGRVKLVHSALIQLGDSLSHKGNEFWGTT QTLNVKFLPSDPNHFIIGTDMGLISHGTRQDL RVAPKLFKPQQHGIRPVKVNVIDFSPFGEPIFL AGCSDGSIRLHQLSSAFPLLQWDSSTDSHAVT GLQWSPTRPAVFLVQDDTSNIYIWDLLQSDL GPVAKQQVSPNRLVAMAAVGEPEKAGGSFL ALVLARASGSIDIQHLKRRWAAPEVDECNRLR LLLQEALWPEGKLHK G17675. 1 250 13 204 8465 MTCPRNVTPNSYAEPLAAPGGGERYSRSAG 1 2 TCGA- MYMQSGSDFNCGVMRGCGLAPSLSKRDEGS 19- SPSLALNTVPSYLSQLDSWGDPKAAYRLEQPV 2624- GRPLSSCSYPPSVKEENVCCMYSAEKRAKSGP 01A- EAALYSHPLPESCLGEHEVPVPSYYRASPSYSA 01R- LDKTPHCSGANDFEAPFEQRASLNPRAEHLES 1850- PQLGGKVSFPETPKSDSQTPSPNEIKTEQSLAG 01.2 PKGSPSESEKERAKAADSSPDTSDNEAKGKYIA STQRPDGTWRKQRRVKEGYVPQEEVPVYEN KYVKFFKSKPELPPGLSPEATAPVTPSRPEGGE PGLSKTAKRNLKRKEKRRQQQEKGEAEALSRT LDKVSLEETAQLPSAPQGSRAAPTAASDQPDS AATTEKAKKIKNLKKKLRQVEELQQRIQAGEVS QPSKEQLEKLARRRALEEELEDLELGL G17803. 1 359 14 425 8466 MAAEKQVPGGGGGGGSGGGGGSGGGGSG 9 2 TCGA- GGRGAGGEENKENERPSAGSKANKEFGDSLS 76- LEILQIIKESQQQHGLRHGDFQRYRGYCSRRQ 4925- RRLRKTLNFKMGNRHKFTGKKVTEELLTDNRY 01A- LLLVLMDAERAWSYAMQLKQEANTEPRKRF 01R- HLLSRLRKAVKHAEELERLCESNRVDAKTKLEA 1850- QAYTAYLSGMLRFEHQEWKAAIEAFNKCKTIY 01.4 EKLASAFTEEQAVLYNQRVEEISPNIRYCAYNI GDQSAINELMQMRLRSGGTEGLLAEKLEALIT QTRAKQAATMSEVEWRGRTVPVKIDKVRIFLL GLADNEAAIVQAESEETKERLFESMLSECRDAI QVVREELKPDQPLISRNYKGDVAMSKIEHFM PLLVQREEEGALAPLLSHGQVHFLWIKHSNLY LVATTSKNANASLVYSFLYKTIEVFCEYFKELEE ESIRDNFVIVYELLDELMDFGFPQTTDSKILQEY ITQQSNKLETGKSRVPPTVTNAVSWRSEGIKY KKNEVFIDVIESVNLLVNANGSVLLSEIVGTIKL KVFLSGMPELRLGLNDRVLFELTGLSGSKNKS VELEDVKFHQCVRLSRFDNDRTISFIPPDGDFE LMSYRLSTQVKPLIWIESVIEKFSHSRVEIMVK AKGQFKKQSVANGVEISVPVPSDADSPRFKTS VGSAKYVPERNVVIWSIKSFPGGKEYLMRAHF GLPSVEKEEVEGRPPIGVKFEIPYFTVSGIQVRY MKIIEKSGYQALPWVRYITQSGDYQLRTS G17796. 1 211 100 350 8467 MSLLRSLRVFLVARTGSYPAGSLLRQSPQPRH 6 2 TCGA- TFYAGPRLSASASSKELLMKLRRKTGYSFVNCK 41- KALETCGGDLKQAEIWLHKEAQKEGWSKAAK 5651- LQRKTKEGLIGLLQEGNTTVLVEVNCETDFV 01A- SRNLKFQLLVQQVALGTMMHCQTLKDQPSA 01R- YSKVQWLTPVNLALWEAEAGGSLEGFLNSSEL 1850- SGLPAGPDREGSLKDQLALAIDSTSAYSSLLTF 01.4 HLSTPRSHHLYHARLWLHVLPTLPGTLCLRIFR WGPRRRRQGSRTLLAEHHITNLGWHTLTLPS SGLRGEKSGVLKLQLDCRPLEGNSTVTGQPRR LLDTAGHQQPFLELKIRANEPGAGRARRRTPT CEPATPLCCRRDHYVDFQELGWRDWILQPEG YQLNYCSGQCPPHLAGSPGIAASFHSAVFSLLK ANNPWPASTSCCVPTARRPLSLLYLDHNGNV VKTDVPDMVVEACGCS G17663. 1 140 585 1374 8468 MASLRRVKVLLVLNLIAVAGFVLFLAKCRPIAV 2 5 TCGA- RSGDAFHEIRPRAEVANLSAHSASPIQDAVLK 19- RLSLLEDIVYRQLNGLSKSLGLIEGYGGRGKGG 2619- LPATLSPAEEEKAKGPHEKYGYNSYLSEKISLDR 01A- SIPDYRPTKFVIGREKPGQVSEVAQLISQTLEQ 01R- ERRQRELLEQHYAQYDADDDENTVAELQGM 1850- SGNCNNNNNYFLKTGEYATDEEEDEVGPVLP 01.2 GSDMAIEVFELPENEDMFSPSELDTSKLSHKF KELQIKHAVTEAEIQKLKTKLQAAENEKVRWE LEKTQLQQNIEENKERMLKLESYWIEAQTLCH TVNEHLKETQSQYQALEKKYNKAKKLIKDFQQ KELDFIKRQEAERKKIEDLEKAHLVEVQGLQVR IRDLEAEVFRLLKQNGTQVNNNNNIFERRTSL GEVSKGDTMENLDGKQTSCQDGLSQDLNEA VPETERLDSKALKTRAQLSVKNRRQRPSRTRLY DSVSSTDGEDSLERKPSNSFYNHMHITKLLPPK GLRTSSPESDSGVPPLTPVDSNVPFSSDHIAEF QEEPLDPEMGPLSSMWGDTSLFSTSKSDHDV EESPCHHQTTNKKILREKDDAKDPKSLRASSSL AVQGGKIKRKFVDLGAPLRRNSSKGKKWKEK EKEASRFSAGSRIFRGRLENWTPKPCSTAQTST RSPCMPFSWFNDS6RKGSYSFRNLPAPTSSLQP SPETLISDKKGSKVENTWITKANKRNPNPSSSS IFGRHSQLMSVVWIQETNNFTFNDDFSPSSTS SADLSGLGAEPKTPGLSQSLALSSDEILDDGQS PKHSQCQNRAVQEWSVQQVSHWLMSLNLE QYVSEFSAQNITGEQLLQLDGNKLKALGMTA SQDRAVVKKKLKEMKMSLEKARKAQEKMEK QREKLRRKEQEQMQRKSKKTEKMTSTTAEGA GEQ G17207. 1 2 205 925 8469 MQSTQAHENSRDSRLAWMGTWEHLVSTGF 1 8 TCGA- NQMREREVKLWDTRFFSSALASLTLDTSLGCL 06- VPLLDPDSGLLVLAGKGERQLYCYEVVPQQPA 0156- LSPVTQCVLESVLRGAALVPRQALAVMSCEVL 01A- RVLQLSDTAIVPIGYHVPRKAVEFHEDLFPDTA 03R- GCVPATDPHSWWAGDNQQVQKVSLNPACR 1849- PHPSFTSCLVPPAEPLPDTAQPAVMETPVGD 01.2 ADASEGFSSPPSSLTSPSTPSSLGPSLSSTSGIGT SPSLRSLQSLLGPSSKFRHAQGTVLHRDSHITN LKGLNLTTPGESDGFCANKLRVAVPLLSSGGQ VAVLELRKPGRLPDTALPTLQNGAAVTDLAW DPFDPHRLAVAGEDARIRLWRVPAEGLEEVLT TPETVLTGHTEKICSLRFHPLAANVLASSSYDLT VRIWDLQAGADRLKLQGHQDQIFSLAWSPD GQQLATVCKDGRVRVYRPRSGPEPLQEGPGP KGGRGARIVWVCDGRCLLVSGFDSQSERQLL LYEAEALAGGPLAVLGLDVAPSTLLPSYDPDTG LVLLTGKGDTRVFLYELLPESPFFLECNSFTSPD PHKGLVLLPKTECDVREVELMRCLRLRQSSLEP VAFRLPRVRKEFFQDDVFPDTAVIWEPVLSAE AWLQGANGQPWLLSLQPPDMSPVSQAPRE APARRAPSSAQYLEEKSDQQKKEELLNAMVA KLGNREDPLPQDSFEGVDEDEWD G17802. 1 68 190 225 8470 MGETMSKRLKLHLGGEAEMEERAFVNPFPDY 1 6 TCGA- EAAAGALLASGAAEETGCVRPPATTDEPGLPF 28- HQDGKDAFIGFGGNVIRQQVKDNAKWYITD 5208- FVELLGELEE 01A- 01R- 1850- 01.4 G17485. 1 17 156 569 8471 MPQSKSRKIAILGYRSVASGLSSSPSTPTQVTK 1 4 TCGA- QHTFPLESYKHEPERLENRIYASSSPPDTGQRF 14- CPSSFQSPTRPPLASPTHYAPSKAAALAAALGP 1402- AEAGMLEKLEFEDEAVEDSESGVYMRFMRSH 02A- KCYDIVPTSSKLVVFDTTLQVKKAFFALVANGV 01R- RAAPLWESKKQSFVGMLTITDFINILHRYYKSP 2005- MVQIYELEEHKIETWRELYLQETFKPLVNISPD 01.2 ASLFDAVYSLIKNKIHRLPVIDPISGNALYILTHK RILKFLQLFMSDMPKPAFMKQNLDELGIGTYH NIAFIHPDTPIIKALNIFVERRISALPVVDESGKV VDIYSKFDVINLAAEKTYNNLDITVTQALQHRS QYFEGVVKCNKLEILETIVDRIVRAEVHRLVVV NEADSIVGIISLSDILQALILTPAGAKQKETETE NYU_E 1 252 68 211 8472 MGAGPSLLLAALLLLLSGDGAVRCDTPANCTY 5 2 LDLLGTWVFQVGSSGSQRDVNCSVMGPQEK KVVVYLQKLDTAYDDLGNSGHFTIIYNQGFEIV LNDYKWFAFFKYKEEGSKVTTYCNETMTGWV HDVLGRNWACFTGKKVGTASENVYVNIAHLK NSQEKYSNRLYKYDHNFVKAINAIQKSWTATT YMEYETLTLGDMIRRSGGHSRKIPRPKPAPLT AEIQQKILHLPTSWDWRNVHGINFVSPVRNQ GQERFGNMTRVYYREAMGAFIVFDVTRPATF EAVAKWKNDLDSKLSLPNGKPVSVVLLANKC DQGKDVLMNNGLKMDQFCKEHGFVGWFET SAKENINIDEASRCLVKHILANECDLMESIEPD VVKPHLTSTKVASCSGCAKS G17212. 1 1367 15 338 8473 MAERGLEPSPAAVAALPPEVRAQLAELELELS 34 2 TCGA- EGDITQKGYEKKRSKLLSPYSPQTQETDSAVQ 06- KELRNQTPAPSAAQTSAPSKYHRTRSGGARD 0129- ERYRSDIHTEAVQAALAKHKEQKMALPMPTK 01A- RRSTFVQSPADACTPPDTSSASEDEGSLRRQA 01R- ALSAALQQSLQNAESWINRSIQGSSTSSSASST 1849- LSHGEVKGTSGSLADVFANTRIENFSAPPDVT 01.2 TTTSSSSSSSSIRPANIDLPPSGIVKGMHKGSN RSSLMDTADGVPVSSRVSTKIQQLLNTLKRPK RPPLKEFFVDDSEEIVEVPQPDPNQPKPEGRQ MTPVKGEPLGVICNWPPALESALQRWGTTQ AKCSCLTALDMTGKPVYTLTYGKLWSRSLKLA YTLLNKLGTKNEPVLKPGDRVALVYPNNDPV MFMVAFYGCLLAEVIPVPIEVPLTRKDAGGQ QIGFLLGSCGIALALTSEVCLKGLPKTQNGEIV QFKGWPRLKWVVTDSKYLSKPPKDWQPHISP AGTEPAYIEYKTSKEGSVMGVTVSRLAMLSHC QALSQACNYSEGETIVNVLDFKKDAGLWHG MFANVMNKMHTISVPYSVMKTCPLSWVQR VHAHKAKVALVKCRDLHWAMMAHRDQRD VSLSSLRMLIVTDGANPWSVSSCDAFLSLFQS HGLKPEAICPCATSAEAMTVAIRRPGVPGAPL PGRAILSMNGLSYGVIRVNTEDKNSALTVQDV GHVMPGGMMCIVKPDGPPQLCKTDEIGEICV SSRTGGMMYFGLAGVTKNTFEVIPVNSAGSP VGDVPFIRSGLLGFVGPGSLVFVVGKMDGLL MVSGRRHNADDIVATGLAVESIKTVYRGRIAV FSVSVFYDERIVVVAEQRPDASEEDSFQWMS RVLQAIDSIHQVGVYCLALVPANTLPKTPLGGI HISQTKQLFLEGSLHPCNILMCPHTCVTNLPKP RQKQPGVGPASVMVGNLVAGKRIAQAAGRD LGQIEENDLVRKHQFLAEILQWRAQATPDHV LFMLLNAKGTTVCTASCLQLHKRAERIASVLG DKGHLNAGDNVVLLYPPGIELIAAFYGCLYAG CIPVTVRPPHAQNLTATLPTVRMIVDVSKAAC ILTSQTLMRLLRSREAAAAVDVKTWPTIIDTDD LPRKRLPQLYKPPTPEMLAYLDFSVSTTGMLT GVKMSHSAVNALCRAIKLQCELYSSRQIAICLD PYCGLGFALWCLCSVYSGHQSVLIPPMELENN LFLWLSIVNQYKIRDTFCSYSVMELCTKGLGN QVEVLKTRGINLSCVRTCVVVAEERPRVALQQ SFSKLFKDIGLSPRAVSTTFGSRVNVAICLQGTS GPDPTTVYVDLKSLRHDRVRLVERGAPQSLLL SESGKRSGSKQSTNPADNYHLARRRTLQVVVS SLLTEAGFESAEKASVETLTEMLQSYISEIGRSA KSYCEHTARTQPTLSDIVVTLVEMGFNVDTLP AYAKRSQRMVITAPPVTNQPVTPKALTAGQN RPHPPHIPSHFPEFPDPHTYIKTPTYREPVSDY QVLREKAASQRRDVERALTRFMAKTGETQSL FKDDVSTFPLIAARPFTIPYLTALLPSELEMQQ MEETDSSEQDEQTDTENLALHISMIESRSVTQ AGVQWQDLGSLQPPPPGFKRFSSLSLLSSWN YRRILEPRRRTPLSCSRTPPCRVAGMGRRTSSI TLICGR G17787. 1 337 376 601 8474 MEPPAAKRSRGCPAGPEERDAGAGAARGRG 5 7 TCGA- RPEALLDLSAKRVAESWAFEQVEERFSRVPEP 26- VQKRIVFWSFPRSEREICMYSSLGYPPPEGEH 5139- DARVPFTRGLHLLQSGAVDRVLQVGFHLSGNI 01A- REPGSPGEPERLYHVSISFDRCKITSVSCGCDN 01R- RDLFYCAHVVALSLYRIRHAHQVELRLPISETLS 1850- QMNRDQLQKFVQYLISAHHTEVLPTAQRLAD 01.4 EILLLGSEINLVNGAPDPTAGAGIEDANCWHL DEEQIQEQVKQLLSNGGYYGASQQLRSMFSK VREMLRMRDSNGARMLILMTEQFLQDTRLA LWRQQGAGMTDKCRQLWDELGMFNSPEM QALLQQISENPQLMQNVISAPYMRSMMQTL AQNPDFAAQMMVNVPLFAGNPQLQEQLRL QLPVFLQQMQNPESLSILTNPRAMQALLQIQ QGLQTLQTEAPGLVPSLGSFGISRTPAPSAGS NAGSTPEAPTSSPATPATSSPTGASSAQQQL MQQMIQLLAGSGNSQVQTPEVRFQQQLEQL NSMGFINREANLQALIATGGDINAAIERLLGS QLS G17675. 1 473 82 514 8475 MDVLPTGGGRPGLRTELEFRGGGGEARLESQ 8 2 TCGA- EEETIPAAPPAPRLRGAAERPRRSRDTWDGDE 19- DTEPGEACGGRTSRTASLVSGLLNELYSCTEEE 2624- EAAGGGRGAEGRRRRRDSLDSSTEASGSDVV 01A- LGGRSGAGDSRVLQELQERPSQRHQMLYLR 01R- QKDANELKTILRELKYRIGIQSAKLLRHLKQKDR 1850- LLHKVQRNCDIVTACLQAVSQKRRVDTKLKFT 01.2 LEPSLGQNGFQQWYDALKAVARLSTGIPKEW RRKVWLTLADHYLHSIAIDWDKTMRFTFNER SNPDDDSMGIQIVKDLHRTGCSSYCGQEAEQ DRVVLKRVLLAYARWNKTVGYCQGFNILAALI LEVMEGNEGDALKIMIYLIDKVLPESYFVNNLR ALSVDMAVFRDLLRMKLPELSQHLDTLQRTA NKESGGGYEPPLTNVFTMQWFLTLFATCLPN QTVLKIWDSVFFEGSEIILRVSLAIWAKLGEVIN AGKSTHNEDQASCEVLTVKKKAGAVTSTPNR NSSKRRSSLPNGEGLQLKENSESEGVSCHYWS LFDGHAGSGAAVVASRLLQHHITEQLQDIVDI LKNSAVLPPTCLGEEPENTPANSRTLTRAASLR GGVGAPGSPSTPPTRFFTEKKIPHECLVIGALE SAFKEMDLQIERERSSYNISGGCTALIVICLLGK LYVANAGDSRAIIIRNGEIIPMSSEFTPETERQR LQYLAFMQPHLLGNEFTHLEFPRRVQRKELGK KMLYRDFNMTGWAYKTIEDEDLKFPLIYGEGK KARVMATIGVTRGLGDHDLKVHDSNIYIKPFL SSAPEVRIYDLSKYDHGSDDVLILATDGLWDVL SNEEVAEAITQFLPNCDPDDPHRYTLAAQDLV MRARGVLKDRGWRISNDRLGSGDDISVYVIPL IHGNKLS G17800. 1 318 97 104 8476 MDNMSITNTPTSNDACLSIVHSLMCHRQGG 7 2 TCGA- ESETFAKRAIESLVKKLKEKKDELDSLITAITTNG 06- AHPSKCVTIQRTLDGRLQVAGRKGFPHVIYAR 5859- LWRWPDLHKNELKHVKYCQYAFDLKCDSVCV 01A- NPYHYERVVSPGIDLSGLTLQSNAPSSMMVK 01R- DEYVHDFEGQPSLSTEGHSIQTIQHPPSNRAS 1849- TETYSTPALLAPSESNATSTANFPNIPVASTSQ 01.4 PASILGGSHSEGLLQIASGPQPGQQQNGFTG QPATYHHNSTTTWTGSRTAPYTPNLPHHQN GHLQHHPPMPPHPGHYWPVHNELAFQPPIS NHPGVVPEPTG G17638. 1 116 70 211 8477 MAAAAGAPPPGPPQPPPPPPPEESSDSEPEA 3 3 TCGA- EPGSPQKLIRKVSTSGQIRQKTIIKEGMLTKQN 28- NSFQRSKRRYFKLRGRTLYYAKTAKSIIFDEVDL 2499- TDASVAESSTKNVNNSFTVEVLDENNLVMNL 01A- EFSIRETTCRKDSGEDPATCAFQRDYYVSTAVC 01R- RSTVKVSAQQVQGVHARCSWSSSTSESYSSEE 1850- MIFGDMLGSHKWRNNYLFGLISDESISEQFYD 01.2 RSLGIMRRVLPPGNRRYPNHRHRARINTDFE

Annotation information in each column is described below for Table 7:

sample: Name of TCGA or private sample. #chrom5p: 5′ chromosome #start5p: 5′ genomic start coordinate #end5p: 5′ genomic end coordinate #chrom3p: 3′ chromosome #start3p: 3′ genomic start coordinate #end3p: 3′ genomic end coordinate strand5p: 5′ strand strand3p: 3′ strand genes5p: 5′ gene genes3p: 3′ gene total_frags (split inserts+split reads): Total number of split inserts and split reads spanning_frags (split reads): Number of split reads GeneBreakpoint5p: The genomic coordinate of the breakpoint in the 5′ gene GeneBreakpoint3p: The genomic coordinate of the breakpoint in the 3′ gene FrameType: Reading frame of gene fusions. Values include in-frame, frameshift, or null (no transcript information was found in the Ensembl Homo_sapiens.GRCh37.60.gtf file). FusedSequence: Reconstructed sequence of the fusion RNA transcript ProteinStart5p: The start coordinate of the 5′ protein segment ProteinStop5p: The stop coordinate (breakpoint) of the 5′ protein segment ProteinStart3p: The start coordinate (breakpoint) of the 3′ protein segment ProteinStop3p: The stop coordinate of the 3′ protein segment ProteinSequence: Reconstructed sequence of the fusion protein ExonBreak5p: The last exon of the 5′ gene before the breakpoint ExonBreak3p: The first exon of the 3′ gene after the breakpoint

Table 8. Genomic breakpoints of gene fusions detected through whole-exome DNA sequencing. Annotation information in each column is described below:

Table 8. Genomic breakpoints of gene fusions detected through whole-exome DNA sequencing. Annotation information in each column is described below:

TABLE 8 Genomic breakpoints of gene fusions detected through whole-exome DNA sequencing. Annotation information in each column is described below: Exon Before split Sense Breakpoint Break sample reads gene5p chr5p 5p Start 5p End 5p 5p point 5p TCGA-06-0750- 51 EGFR chr7 + 55054218 55268221 55268221 24 01A-01D-1492- 08 TCGA-27-1837- 648 EGFR chr7 + 55086724 55268937 55268937 24 01A-01D-1494- 08 TCGA-28-2513- 378 EGFR chr7 + 55086724 55269001 55269001 24 01A-01D-1494- 08 TCGA-06-5411- 676 NFASC chr1 + 204797781 204951827 204951827 21 01A-01D-1696- 08 TCGA-32-5222- 0 EGFR chr7 + 55086724 N/A N/A N/A 01A-01D-1486- 08 TCGA-28-5209- 0 EGFR chr7 + 55086724 N/A N/A N/A 01A-01D-1486- 08 Exon After split Gene Sense Breakpoint Break sample reads 3p chr3p 3p start3p end3p 3p point 3p TCGA-06-0750- 51 SEPT14 chr7 − 55828730 55871487 55871487 10 01A-01D-1492- 08 TCGA-27-1837- 648 SEPT14 chr7 − 55861236 55870909 55870909 10 01A-01D-1494- 08 TCGA-28-2513- 378 SEPT14 chr7 − 55861236 55871369 55871369 10 01A-01D-1494- 08 TCGA-06-5411- 676 NTRK1 chr1 + 156844170 156851642 156844170 10 01A-01D-1696- 08 TCGA-32-5222- 0 SEPT14 chr7 − 55861236 N/A N/A N/A 01A-01D-1486- 08 TCGA-28-5209- 0 PSPH chr7 − 56078743 N/A N/A N/A 01A-01D-1486- 08 Read split Dir sample inserts posA5p posB5p 5p posA3p posB3p readDir 3p TCGA-06- 17 55242336 55268011 Fwd 55871183 55871412 Fwd 0750-01A- 01D-1492-08 TCGA-27- 505 55268346 55268884 Fwd 55870367 55870871 Fwd 1837-01A- 01D-1494-08 TCGA-28- 251 55268377 55268962 Fwd 55871008 55871339 Fwd 2513-01A- 01D-1494-08 TCGA-06- 131 204951788 204951826 Fwd 156844171 156844232 Rev 5411-01A- 01D-1696-08 TCGA-32- 1 55628015 55628015 Fwd 55872287 55872287 Fwd 5222-01A- 01D-1486-08 TCGA-28- 1 55198162 55198162 Rev 56087184 56087184 Fwd 5209-01A- 01D-1486-08 Annotation information in each column is described below for Table 8: sample: Name of TCGA sample split reads: Total number of split reads gene5p: 5′ gene chr5p: 5′ chromosome sense5p: 5′ sense start5p: 5′ genomic start coordinate end5p: 5′ genomic end coordinate breakpoint5p: 5′ genomic coordinate of breakpoint exonBeforeBreakpoint5p: Exon number of 5′ gene before the breakpoint gene3p: 3′ gene chr3p: 3′ chromosome sense3p: 3′ sense start3p: 3′ genomic start coordinate end3p: 3′ genomic end coordinate breakpoint3p: 3′ genomic coordinate of breakpoint exonAfterBreakpoint3p: Exon number of 3′ gene after the breakpoint split inserts: Total number of split inserts posA5p: Coordinate of split insert read closest to 5′ end in 5′ gene posB5p: Coordinate of split insert read closest to 3′ end in 5′ gene readDir5p: Read direction of split insert reads in 5′ gene posA3p: Coordinate of split insert read closest to 5′ end in 3′ gene posB3p: Coordinate of split insert read closest to 3′ end in 3′ gene readDir3p: Read direction of split insert reads in 3′ gene

TABLE 11 Relative expression of EGFR fusion and wild-type transcripts. Expression is estimated using the depth of reads covering the fusion breakpoint or wild-type exon junctions excluded from the fusion transcript. These wild-type exons include exons 25-26, 26-27, and 27-28. Fusion Sample Bp Exon 25-26 Exon 26-27 Exon 27-28 EGFR-SEPT14 TCGA-28-2513 1464 21 12 25 TCGA-27-1837 796 6 5 6 TCGA-06-0750 414 69 61 101 TCGA-32-5222 495 256 190 348 TCGA-28-1747 142 426 300 502 TCGA-06-2557 13 1031 657 1254 EGFR-PSPH TCGA-28-5209 5648 216 122 232 TCGA-06-5408 37 232 200 292 TCGA-28-5215 28 29 26 44

TABLE 12 Genomic breakpoints of gene fusions detected through whole-exome DNA sequencing. Exon Before Break- split Gene Chr Sense Break point sample reads 5p 5p 5p Start 5p End 5p point 5p 5p TCGA-06- 51 EGFR chr7 + 55054218 55268221 55268221 24 0750-01A- 01D-1492- 08 TCGA-27- 648 EGFR chr7 + 55086724 55268937 55268937 24 1837-01A- 01D-1494- 08 TCGA-28- 378 EGFR chr7 + 55086724 55269001 55269001 21 2513-01A- 01D-1494- 08 TCGA-06- 676 NFASC chr1 + 204797781 204951827 204951827 21 5411-01A- 01D-1696- 08 TCGA-32- 0 EGFR chr7 + 55086724 N/A N/A N/A 5222-01A- 01D-1486- 08 TCGA-28- 0 EGFR chr7 + 55086724 N/A N/A N/A 5209-01A- 01D-1486- 08 Exon After Gene Sense Break- Break- sample 3p Chr 3p 3p Start 3p End 3p point 3p point 3p TCGA-06- SEPT14 chr7 − 55828730 55871487 55871487 10 0750-01A- 01D-1492- 08 TCGA-27- SEPT14 chr7 − 55861236 55870909 55870909 10 1837-01A- 01D-1494- 08 TCGA-28- SEPT14 chr7 − 55861236 55871369 55871369 10 2513-01A- 01D-1494- 08 TCGA-06- NTRK1 chr1 + 156844170 156851642 156844170 10 5411-01A- 01D-1696- 08 TCGA-32- SEPT14 chr7 − 55861236 N/A N/A N/A 5222-01A- 01D-1486- 08 TCGA-28- PSPH chr7 − 56078743 N/A N/A N/A 5209-01A- 01D-1486- 08 Read split Dir Read sample inserts posA 5p posB 5p 5p posA 3p posB 3p Dir 3p TCGA-06- 17 55242336 55268011 Fwd 55871183 55871412 Fwd 0750-01A- 01D-1492-08 TCGA-27- 505 55268346 55268884 Fwd 55870367 55870871 Fwd 1837-01A- 01D-1494-08 TCGA-28- 251 55268377 55268962 Fwd 55871008 55871339 Fwd 2513-01A- 01D-1494-08 TCGA-06- 131 204951788 204951826 Fwd 156844171 156844232 Fwd 5411-01A- 01D-1696-08 TCGA-32- 1 55268015 55268015 Fwd 55872287 55872287 Fwd 5222-01A- 01D-1486-08 TCGA-28- 1 55198162 55198162 Rev 56087184 56087184 Fwd 5209-01A- 01D-1486-08 Annotation information in each column is described below for Table 12: sample: Name of TCGA sample split reads: Total number of split reads gene5p: 5′ gene chr5p: 5′ chromosome sense5p: 5′ sense start5p: 5′ genomic start coordinate end5p: 5′ genomic end coordinate breakpoint5p: 5′ genomic coordinate of breakpoint exonBeforeBreakpoint5p: Exon number of 5′ gene before the breakpoint gene3p: 3′ gene chr3p: 3′ chromosome sense3p: 3′ sense start3p: 3′ genomic start coordinate end3p: 3′ genomic end coordinate breakpoint3p: 3′ genomic coordinate of breakpoint exonAfterBreakpoint3p: Exon number of 3′ gene after the breakpoint split inserts: Total number of split inserts posA5p: Coordinate of split insert read closest to 5′ end in 5′ gene posB5p: Coordinate of split insert read closest to 3′ end in 5′ gene readDir5p: Read direction of split insert reads in 5′ gene posA3p: Coordinate of split insert read closest to 5′ end in 3′ gene posB3p: Coordinate of split insert read closest to 3′ end in 3′ gene readDir3p: Read direction of split insert reads in 3′ gene.

TABLE 13 Analysis of the incidence of EGFR-SEPT14 and EGFR-PSPH gene fusions in GBM harboring or not the EGFRvIII rearrangement. EGFR- Isoform EGFR-SEPT14 PSPH Non-Fusion Total EGFRvIII 1 1 14 16 No EGFRvIII 5 2 64 71 Total 6 3 78 87

TABLE 14 Enrichment of classical/mesenchymal subtype among samples with EGFR-SEPT14 or EGFR-PSPH. Classical Mesenchymal Proneural Neural EGFR 3 5 1 0 Fusion No Fusion 37 47 38 0 Total 40 52 39 28 Fisher's p-value = 0.0500 for the enrichment of classical/mesenchymal subtype

TABLE 15 Antibodies and concentrations used in immunofluorescence staining. B-III Tubulin Mouse 1:400 Promega δ-Catenin Guinea 1:500 Acris Pig Fibronectin Mouse 1:1000 BD- Pharmingen Col5A1 Rabbit 1:200 Santa Cruz Biotech PSD-95 Rabbit 1:500 Invitrogen Smooth muscle Mouse 1:200 Sigma actin

TABLE 16 Antibodies and concentrations used for Western blots and immunopreciptation assays. Anti-Vinculin Mouse 1:400 SIGMA Anti-N-Cadherin Mouse 1:200 BD- Pharmingen Cyclin A Rabbit 1:500 Santa Cruz Biotech p27 Mouse 1:250 BD Transduction B-III Tubulin Mouse 1:400 Promega δ-Catenin Guinea 1:500 Acris Pig Fibronectin Mouse 1:1000 BD- Pharmingen p107 Rabbit 1:1000 Santa Cruz Biotech Nestin Mouse 1:500 BD- Pharmingen CD133 Rabbit 1:200 Abcam Sox2 Rabbit 1:500 Cell Signaling EGFR Mouse 1:1000 Millipore AKT Rabbit 1:1000 Cell Signaling pAKT-S473 Rabbit 1:1000 Cell Signaling ERK1/2 Rabbit 1:1000 Cell Signaling pERK1/2 Rabbit 1:1000 Cell Signaling STAT3 Rabbit 1:1000 Santa Cruz Biotech pSTAT3-Y705 Rabbit 1:1000 Cell Signaling LZTR1 Rabbit 1:1000 Abcam Cul3 Rabbit 1:1000 Bethyl

TABLE 17 Primers used for screening gene fusions from cDNA. SEQ ID Primer NO: Sequence hEGFR-RT-FW1 32 5′- GGGTGACTGTTTGGGAGTTGATG -3 hSEP14-RT-REV1 33 5′- TGTTTGTCTTTCTTTGTATCGGTGC-3′ hEGFR-RT-FW1 87 5′-AGAGGTGACCACCAATCAGC-3′ hPSPH-RT-REV1 88 5′-CGTGTCCCACACAGAGACAG-3′ hNFASC-RT-FW1 36 5′- AGTTCCGTGTCATTGCCATCAAC-3′ hNTRK1-RT-REV1 37 5′- TGTTTCGTCCTTCTTCTCCACCG-3′ hCAND1-RT- FW1 38 5′-GGAAAAAATGACATCCAGCGAC-3′ hEGFR-RT-REV1 39 5′- TGGGTGTAAGAGGCTCCACAAG-3′

TABLE 18 Primers used for genomic detection of gene fusions. SEQ ID Primer NO: Sequence genomic 40 5′- GGATGATAGACGCAGATAGTCGCC-3′ EGFR-FW1 genomic 41 5′- TCCAGTTGTTTTTTCTCTTCCTCG-3′ SEPT14-REV1 genomic 12 5′- TCCGAGTCCAGGCTGAAAATG-3′ NFASC-FW1 genomic 89 5′- CTACTTCCTATCTCACCCCAAAAGG-3′ NTRK1-REV1 genomic 44 5′- GCAATAGCAAAACAGGAAGATGTC-3′ CAND1-FW1 genomic 45 5′- GAACACTTACCCATTCGTTGG-3′ EGFR-REV1

TABLE 19 Primers used for semiquantitative RT-PCR to detect exogenous Myc-LZTR1 WT and mutant LZTR1-R801W. SEQ ID Primer NO: Sequence LZTR1 FW 90 5′- TCCCACATCTCAGACAAGCA-3′ His-Tag REV 91 5′- TCAATGGTGATGGTGATGATG-3′ GAPDH FW 92 5′- GAAGGTGAAGGTCGGAGTCAAC-3′ GAPDH REV 93 5′-CAGAGTTAAAAGCAGCCCTGGT-3′ 

What is claimed is:
 1. A cDNA encoding a fusion protein comprising the tyrosine kinase domain of EGFR fused to: (i) the coiled-coil domain of a Septin protein; (ii) a phosphoserine phosphatase (PSPH) protein; or (iii) a Cullin-associated and neddylation-dissociated (CAND) protein.
 2. The cDNA of claim 1, wherein the Septin protein is Septin-1, Septin-2, Septin-3, Septin-4, Septin-5, Septin-6, Septin-7, Septin-8, Septin-9, Septin-10, Septin-11, Septin-12, Septin-13, or Septin-14
 3. The cDNA of claim 1, wherein the Septin protein is Septin-14 (SEPT14).
 4. The cDNA of claim 1, wherein the CAND protein is CAND protein is CAND1, CAND2, or CAND3.
 5. The cDNA of claim 1, wherein the CAND protein is CAND1.
 6. The cDNA of claim 1, wherein the fusion protein is EGFR-SEPT14, EGFR-CAND1, or EGFR-PSPH.
 7. The cDNA of claim 1, wherein the cDNA comprising the tyrosine kinase domain of EGFR fused to the coiled-coil domain of a Septin protein comprises SEQ ID NO: 2, or SEQ ID NO: 4 or has a genomic breakpoint comprising SEQ ID NO:
 4. 8. The cDNA of claim 1, wherein the cDNA comprising the tyrosine kinase domain of EGFR fused to a PSPH protein comprises SEQ ID NO: 8 or SEQ ID NO: 10 or has a genomic breakpoint comprising SEQ ID NO:
 10. 9. The cDNA of claim 1, wherein the cDNA comprising the tyrosine kinase domain of EGFR fused to a CAND protein comprises SEQ ID NO: 14 or SEQ ID NO: 15, or has a genomic breakpoint comprising SEQ ID NO:
 15. 10. A purified fusion protein comprising the tyrosine kinase domain of EGFR fused to: (i) the coiled-coil domain of a Septin protein; (ii) a phosphoserine phosphatase (PSPH) protein; or (iii) a Cullin-associated and neddylation-dissociated (CAND) protein.
 11. The purified fusion protein of claim 10, wherein the fusion protein is EGFR-SEPT14, EGFR-CAND1, or EGFR-PSPH.
 12. The purified fusion protein of claim 10, wherein the fusion protein comprises SEQ ID NO: 1, 5, 7, 11, 13, or
 8495. 13. An antibody or antigen-binding fragment thereof, that specifically binds to a purified fusion protein comprising a tyrosine kinase domain of an EGFR protein fused to a polypeptide comprising: (i) the coiled-coil domain of a Septin protein; (ii) a phosphoserine phosphatase (PSPH) protein; or (iii) a Cullin-associated and neddylation-dissociated (CAND) protein.
 14. The antibody or antigen-binding fragment of claim 13, wherein the Septin protein is SEPT14.
 15. The antibody or antigen-binding fragment of claim 13, wherein the CAND protein is CAND1.
 16. The antibody or antigen-binding fragment of claim 13, wherein the fusion protein is EGFR-SEPT14, EGFR-CAND1, or EGFR-PSPH.
 17. The antibody or antigen-binding fragment of claim 13, wherein the EGFR-SEPT14 fusion protein comprises the amino acid sequence of SEQ ID NO: 1, 3, or
 5. 18. The antibody or antigen-binding fragment of claim 13, wherein the EGFR-CAND1 fusion protein comprises the amino acid sequence of SEQ ID NO: 13, 16, or
 8495. 19. The antibody or antigen-binding fragment of claim 13, wherein the EGFR-PSPH fusion protein comprises the amino acid sequence of SEQ ID NO: 7, 9, or
 11. 20. A composition for decreasing the expression level or activity of a fusion protein in a subject comprising the tyrosine kinase domain of an EGFR protein fused to a polypeptide comprising: (i) the coiled-coil domain of a Septin protein; (ii) a phosphoserine phosphatase (PSPH) protein; or (iii) a Cullin-associated and neddylation-dissociated (CAND) protein; the composition in an admixture of a pharmaceutically acceptable carrier comprising an inhibitor of the fusion protein.
 21. The composition of claim 20, wherein the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof.
 22. The composition of claim 20, wherein the fusion protein is EGFR-SEPT14, EGFR-CAND 1, or EGFR-PSPH.
 23. The composition of claim 21, wherein the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.
 24. A method of decreasing growth of a solid tumor in a subject in need thereof, the method comprising administering to the subject an effective amount of an EGFR fusion molecule inhibitor, wherein the inhibitor decreases the size of the solid tumor, and wherein the EGFR fusion comprises the tyrosine kinase domain of EGFR fused to: (i) the coiled-coil domain of a Septin protein; (ii) a phosphoserine phosphatase (PSPH) protein; or (iii) a Cullin-associated and neddylation-dissociated (CAND) protein.
 25. The method of claim 24, wherein the solid tumor comprises glioblastoma multiforme, breast cancer, lung cancer, prostate cancer, or colorectal carcinoma.
 26. The method of claim 24, wherein the inhibitor comprises an antibody that specifically binds to an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion protein, or a fragment thereof; a small molecule that specifically binds to an EGFR protein; an antisense RNA or antisense DNA that decreases expression of an EGFR-SEPT fusion protein, an EGFR-PSPH fusion protein, an EGFR-CAND fusion; a siRNA that specifically targets an EGFR-SEPT fusion gene, an EGFR-PSPH fusion gene, or an EGFR-CAND; or a combination thereof.
 27. The method of claim 24, wherein the fusion protein is EGFR-SEPT14, EGFR-CAND 1, or EGFR-PSPH.
 28. The method of claim 26, wherein the small molecule that specifically binds to an EGFR protein comprises AZD4547, NVP-BGJ398, PD173074, NF449, TK1258, BIBF-1120, BMS-582664, AZD-2171, TSU68, AB1010, AP24534, E-7080, LY2874455, or a combination thereof.
 29. A diagnostic kit for determining whether a sample from a subject exhibits a presence of an EGFR fusion, the kit comprising at least one oligonucleotide that specifically hybridizes to an EGFR fusion, or a portion thereof, wherein the EGFR fusion comprises the tyrosine kinase domain of EGFR fused to: (i) the coiled-coil domain of a Septin protein; (ii) a phosphoserine phosphatase (PSPH) protein; or (iii) a Cullin-associated and neddylation-dissociated (CAND) protein.
 30. The kit of claim 29, wherein the oligonucleotides comprise a set of nucleic acid primers or in situ hybridization probes.
 31. The kit of claim 29, wherein the oligonucleotide comprises SEQ ID NO: 32, 33, 34, 35, 38, 39, 40, 41, 44, 45, 87, or
 88. 32. The kit of claim 30, wherein the primers prime a polymerase reaction only when an EGFR fusion is present.
 33. The kit of claim 29, wherein the fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein.
 34. The kit of claim 29, wherein the determining comprises gene sequencing, selective hybridization, selective amplification, gene expression analysis, or a combination thereof.
 35. A diagnostic kit for determining whether a sample from a subject exhibits a presence of an EGFR fusion protein, the kit comprising an antibody that specifically binds to an EGFR fusion protein comprising SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 16, or 8495, wherein the antibody will recognize the protein only when an EGFR fusion protein is present.
 36. The kit of claim 35, wherein the fusion protein is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein.
 37. A method for detecting the presence of an EGFR fusion in a human subject, the method comprising: (a) obtaining a biological sample from the human subject; and (b) detecting whether or not there is an EGFR fusion present in the subject; wherein the EGFR fusion comprises the tyrosine kinase domain of EGFR fused to: (i) the coiled-coil domain of a Septin protein; (ii) a phosphoserine phosphatase (PSPH) protein; or (iii) a Cullin-associated and neddylation-dissociated (CAND) protein.
 38. The method of claim 37, wherein the detecting comprises measuring EGFR fusion protein levels by ELISA using an antibody directed to SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 16, or 8495; western blot using an antibody directed to SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 16, or 8495; mass spectroscopy, isoelectric focusing, or a combination thereof.
 39. The method of claim 37, wherein the detecting of step (b) comprises detecting whether or not there is a nucleic acid sequence encoding an EGFR fusion protein in the subject.
 40. The method of claim 39, wherein the nucleic acid sequence comprises any one of SEQ ID NOS: 2, 4, 8, 10, 14, or
 15. 41. The method of claim 39, wherein the detecting comprises using hybridization, amplification, or sequencing techniques to detect an EGFR fusion.
 42. The method of claim 41, wherein the amplification uses primers comprising SEQ ID NO: 32, 33, 34, 35, 38, 39, 40, 41, 44, 45, 87, or
 88. 43. The method of claim 37, wherein the EGFR fusion is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein.
 44. The method of claim 39, wherein the EGFR fusion is an EGFR-SEPT14 fusion protein, an EGFR-PSPH fusion protein, or an EGFR-CAND1 fusion protein. 